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US5149806A Expired / Lapsed US ⏱️ 0.0 years remaining

Azlactone michael adducts

Assignee: 3M Co
•
Filing: 1990-03-28
•
Granted: 1992-09-22
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Expires: 2010-03-28
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Abstract

Abstract Azlactone-functional Michael adducts are disclosed which are the Michael reaction products of 2-alkenyl azlactones and Michael donors selected from carbon and nitrogen nucleophiles. Reaction products which contain a plurality of azlactone groups are useful as step growth monomers in adhesives, sealants, and coatings.

Inventors

  • 👤 Dean M. Moren
  • 👤 Steven M. Heilmann
  • 👤 Larry R. Krepski
  • 👤 Jerald K. Rasmussen

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 21:21
CPC Classifications
C; C07; C07D; C07D265/00; C07D265/04; C07D265/06; C07D263/00; C07D263/02; C07D263/30; C07D263/34; C07D263/36; C07D263/42

Claims Analysis

Total Claims: 15
Claim 1
Independent Claim 773 words
An azlactone-functional adduct having the formula ##STR95## wherein p 1 and p 2 independently have integral values of 1 to (the valence of X 1 or X 2 ) -1, where p 1 relates to X 1 and p 2 to X 2 ; R 1 , R 2 , R 7 , and R 8 independently represent an alkyl group, a cycloalkyl group, an aryl group, or at least one of (R 1 and R 2 ) and (R 7 and R 8 ) taken together with the carbon atom to which they are joined form a ring of 4 to 12 atoms; R 3 , R 4 , R 9 , and R 10 are independently hydrogen or lower alkyl; R 5 and R 6 independently are hydrogen or methyl; n 1 and n 2 independently are 0 or 1; X 1 and X 2 independently are selected from the group consisting of --CH 2 (when at least one of p 1 and p 2 =1); --CH (when at least one of p 1 and p 2 =2); --C (when at least one of p 1 and p 2 =3); --CR 11 R 12 in which R 11 and R 12 are selected from the group consisting of alkyl, alkenyl, cycloalkyl, and aryl monovalent groups, a single bond, and polyvalent alkylene, alkenylene, cycloalkylene, or arylene linking groups; --CHR 11 ; --CR 11 ; --CW 1 W 2 in which W 1 and W 2 are independently selected from R 11 O 2 C--, R 11 (CO)--, N.tbd.C--, R F (CO)-- in which R F is a substantially perfluorinated alkyl, cycloalkyl, or aryl group, R 11 NH(CO)--, R 11 R 12 N(CO)--, R 11 SO 2 --, R 11 R 12 C═N--, R 11 N═(R 12 )C--, R 11 (CS)--, R.sup. 11 S 2 C--, R 11 NH(CS)--, R 11 R 12 N(CS)--, R 11 R 12 C═CR 13 -- in which R 13 is defined the same as R 11 and R 12 , and O 2 N-- groups; --CR 11 W 1 ; --CHW 1 ; --CW 1 ; --NR 14 in which R 14 (linking at least one of X 1 to Y 1 , X 1 to G, X 1 to X 2 , X 2 to Y 2 , and X 2 to G) is a single bond, alkylene, alkenylene, or arylene group such that the ring formed contains 4 to 6 ring atoms; and --NW 1 ; Z 1 and Z 2 independently are C, N, or S═O; Y 1 and Y 2 independently are doubly bonded oxygen (═O); doubly bonded sulfur (═S); ═CR 15 R 16 , or --CR 15 ═CR 16 R 17 in which R 15 and R 16 independently are defined the same as R 11 , R 12 , and R 13 , except that R 15 can be an electron pair, and in which R 17 is a monovalent group selected from alkyl, alkenyl, cycloalkyl, and aryl groups; ═NR 15 (to include triply bonded nitrogen (.tbd.N:) when R 15 is an electron pair and G is a single bond from at least one of Y 1 to Z 1 and Y 2 to Z 2 ); or --NR 18 R 19 in which R 18 and R 19 independently can be hydrogen, alkyl, cycloalkyl, aryl, a single bond, alkylene, cycloalkylene, or arylene, or together with the nitrogen atom to which they are joined form a ring of 4 to 12 ring atoms; and G is --H; --NR 20 R 21 in which R 20 and R 21 independently are defined the same as R 11 , R 12 , and R 13 ; --NHR 20 ; --R 20 ; or --OR 20 ; ═O; polymeric monovalent and polyvalent groups; an electron pair; or a single bond; and q is an integer of zero or greater and is equal to (the valence of G)-1; wherein said azlactone-functional adduct is prepared by a process comprising the step of reacting at least one 2-alkenyl azlactone Michael acceptor of Formulae VIIa and VIIb: ##STR96## wherein: R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , n 1 , n 2 , p 1 , and p 2 are as previously defined, with a Michael donor of Formula VIII ##STR97## wherein X 1 , X 2 , Y 1 , Y 2 , Z 1 , Z 2 , G, q, p 1 and p 2 are as previously defined, to provide said azlactone-functional adduct.
Claim 2
Dependent Claim 773 words
An azlactone-functional adduct having the formula ##STR95## wherein p 1 and p 2 independently have integral values of 1 to (the valence of X 1 or X 2 ) -1, where p 1 relates to X 1 and p 2 to X 2 ; R 1 , R 2 , R 7 , and R 8 independently represent an alkyl group, a cycloalkyl group, an aryl group, or at least one of (R 1 and R 2 ) and (R 7 and R 8 ) taken together with the carbon atom to which they are joined form a ring of 4 to 12 atoms; R 3 , R 4 , R 9 , and R 10 are independently hydrogen or lower alkyl; R 5 and R 6 independently are hydrogen or methyl; n 1 and n 2 independently are 0 or 1; X 1 and X 2 independently are selected from the group consisting of --CH 2 (when at least one of p 1 and p 2 =1); --CH (when at least one of p 1 and p 2 =2); --C (when at least one of p 1 and p 2 =3); --CR 11 R 12 in which R 11 and R 12 are selected from the group consisting of alkyl, alkenyl, cycloalkyl, and aryl monovalent groups, a single bond, and polyvalent alkylene, alkenylene, cycloalkylene, or arylene linking groups; --CHR 11 ; --CR 11 ; --CW 1 W 2 in which W 1 and W 2 are independently selected from R 11 O 2 C--, R 11 (CO)--, N.tbd.C--, R F (CO)-- in which R F is a substantially perfluorinated alkyl, cycloalkyl, or aryl group, R 11 NH(CO)--, R 11 R 12 N(CO)--, R 11 SO 2 --, R 11 R 12 C═N--, R 11 N═(R 12 )C--, R 11 (CS)--, R.sup. 11 S 2 C--, R 11 NH(CS)--, R 11 R 12 N(CS)--, R 11 R 12 C═CR 13 -- in which R 13 is defined the same as R 11 and R 12 , and O 2 N-- groups; --CR 11 W 1 ; --CHW 1 ; --CW 1 ; --NR 14 in which R 14 (linking at least one of X 1 to Y 1 , X 1 to G, X 1 to X 2 , X 2 to Y 2 , and X 2 to G) is a single bond, alkylene, alkenylene, or arylene group such that the ring formed contains 4 to 6 ring atoms; and --NW 1 ; Z 1 and Z 2 independently are C, N, or S═O; Y 1 and Y 2 independently are doubly bonded oxygen (═O); doubly bonded sulfur (═S); ═CR 15 R 16 , or --CR 15 ═CR 16 R 17 in which R 15 and R 16 independently are defined the same as R 11 , R 12 , and R 13 , except that R 15 can be an electron pair, and in which R 17 is a monovalent group selected from alkyl, alkenyl, cycloalkyl, and aryl groups; ═NR 15 (to include triply bonded nitrogen (.tbd.N:) when R 15 is an electron pair and G is a single bond from at least one of Y 1 to Z 1 and Y 2 to Z 2 ); or --NR 18 R 19 in which R 18 and R 19 independently can be hydrogen, alkyl, cycloalkyl, aryl, a single bond, alkylene, cycloalkylene, or arylene, or together with the nitrogen atom to which they are joined form a ring of 4 to 12 ring atoms; and G is --H; --NR 20 R 21 in which R 20 and R 21 independently are defined the same as R 11 , R 12 , and R 13 ; --NHR 20 ; --R 20 ; or --OR 20 ; ═O; polymeric monovalent and polyvalent groups; an electron pair; or a single bond; and q is an integer of zero or greater and is equal to (the valence of G)-1; wherein said azlactone-functional adduct is prepared by a process comprising the step of reacting at least one 2-alkenyl azlactone Michael acceptor of Formulae VIIa and VIIb: ##STR96## wherein: R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , n 1 , n 2 , p 1 , and p 2 are as previously defined, with a Michael donor of Formula VIII ##STR97## wherein X 1 , X 2 , Y 1 , Y 2 , Z 1 , Z 2 , G, q, p 1 and p 2 are as previously defined, to provide said azlactone-functional adduct.
Claim 3
Dependent Claim 653 words
An azlactone-functional adduct having the formula ##STR98## wherein p 1 and p 2 independently have integral values of 1 to (the valence of X 1 or X 2 ) -1, where p 1 relates to X 1 and p 2 to X 2 ; R 1 , R 2 , R 7 , and R 8 independently represent an alkyl group, a cycloalkyl group, an aryl group, or at least one of (R 1 and R 2 ) and (R 7 and R 8 ) taken together with the carbon atom to which they are joined form a ring of 4 to 12 atoms; R 3 , R 4 , R 9 , and R 10 are independently hydrogen or lower alkyl; R 5 and R 6 independently are hydrogen or methyl; n 1 and n 2 independently are 0 or 1; X 1 and X 2 independently are selected from the group consisting of --CH 2 (when at least one of p 1 and p 2 =1); --CH (when at least one of p 1 and p 2 =2); --C (when at least one of p 1 and p 2 =3); --CR 11 R 12 in which R 11 and R 12 are selected from the group consisting of alkyl, alkenyl cycloalkyl, and aryl monovalent groups; a single bond; and polyvalent alkylene, alkenylene, cycloalkylene, or arylene linking groups; --CHR 11 ; --CR 11 ; --CW 1 W 2 in which W 1 and W 2 are independently selected from R 11 O 2 C--, R 11 (CO)--, N.tbd.C--, R F (CO)-- in which R F is a substantially perfluorinated alkyl, cycloalkyl, or aryl group, R 11 NH(CO)--, R 11 R 12 N(CO)--, R 11 SO 2 --, R 11 R 12 C═N--, R 11 N═(R 12 )C--, R 11 ( CS)--, R 11 S 2 C--, R 11 NJ(CS)--, R 11 R 12 N(CS)--, R 11 R 12 C═CR 13 -- in which R 13 is defined the same as R 11 and R 12 , and O 2 N-- groups; --CR 11 W 1 ; --CHW 1 ; --CW 1 ; --NR 14 in which R 14 (linking at least one of X 1 to Y 1 , X 1 to G, X 1 to X 2 , X 2 to Y 2 , and X 2 to G) is a single bond, alkylene, alkenylene, or arylene group such that the ring formed contains 4 to 6 ring atoms; and --NW 1 ; Z 1 and Z 2 independently are C; Y 1 and Y 2 independently are doubly bonded oxygen (═O) doubly bonded sulfur (═S); ═CR 15 R 16 , or --CR 15 ═CR 16 R 17 in which R 15 and R 16 independently are defined the same as R 11 , R 12 , and R 13 , except that R 15 can be an electron pair, and in which R 17 is a monovalent group selected from alkyl, alkenyl, cycloalkyl, and aryl groups; ═NR 15 (to include triply bonded nitrogen (.tbd.N:) when R 15 is an electron pair and G is a single bond from at least one of Y 1 to Z 1 and Y 2 to Z 2 ); or --NR 18 R 19 in which R 18 and R 19 independently can be hydrogen, alkyl, cycloalkyl, aryl, a single bond, alkylene, cycloalkylene, or arylene, or together with the nitrogen atom to which they are joined form a ring of 4 to 12 ring atoms; G is --H; --NR 20 R 21 in which R 20 and R 21 independently are defined the same as R 11 , R 12 , and R 13 ; --NHR 20 ; --R 20 ; or --OR 20 ; ═O; polymeric monovalent and polyvalent groups; an electron pair; or a single bond; and q is an integer of 0 or greater and is equal to (the valence of G)-1.
Claim 4
Dependent Claim 653 words
An azlactone-functional adduct having the formula ##STR98## wherein p 1 and p 2 independently have integral values of 1 to (the valence of X 1 or X 2 ) -1, where p 1 relates to X 1 and p 2 to X 2 ; R 1 , R 2 , R 7 , and R 8 independently represent an alkyl group, a cycloalkyl group, an aryl group, or at least one of (R 1 and R 2 ) and (R 7 and R 8 ) taken together with the carbon atom to which they are joined form a ring of 4 to 12 atoms; R 3 , R 4 , R 9 , and R 10 are independently hydrogen or lower alkyl; R 5 and R 6 independently are hydrogen or methyl; n 1 and n 2 independently are 0 or 1; X 1 and X 2 independently are selected from the group consisting of --CH 2 (when at least one of p 1 and p 2 =1); --CH (when at least one of p 1 and p 2 =2); --C (when at least one of p 1 and p 2 =3); --CR 11 R 12 in which R 11 and R 12 are selected from the group consisting of alkyl, alkenyl cycloalkyl, and aryl monovalent groups; a single bond; and polyvalent alkylene, alkenylene, cycloalkylene, or arylene linking groups; --CHR 11 ; --CR 11 ; --CW 1 W 2 in which W 1 and W 2 are independently selected from R 11 O 2 C--, R 11 (CO)--, N.tbd.C--, R F (CO)-- in which R F is a substantially perfluorinated alkyl, cycloalkyl, or aryl group, R 11 NH(CO)--, R 11 R 12 N(CO)--, R 11 SO 2 --, R 11 R 12 C═N--, R 11 N═(R 12 )C--, R 11 ( CS)--, R 11 S 2 C--, R 11 NJ(CS)--, R 11 R 12 N(CS)--, R 11 R 12 C═CR 13 -- in which R 13 is defined the same as R 11 and R 12 , and O 2 N-- groups; --CR 11 W 1 ; --CHW 1 ; --CW 1 ; --NR 14 in which R 14 (linking at least one of X 1 to Y 1 , X 1 to G, X 1 to X 2 , X 2 to Y 2 , and X 2 to G) is a single bond, alkylene, alkenylene, or arylene group such that the ring formed contains 4 to 6 ring atoms; and --NW 1 ; Z 1 and Z 2 independently are C; Y 1 and Y 2 independently are doubly bonded oxygen (═O) doubly bonded sulfur (═S); ═CR 15 R 16 , or --CR 15 ═CR 16 R 17 in which R 15 and R 16 independently are defined the same as R 11 , R 12 , and R 13 , except that R 15 can be an electron pair, and in which R 17 is a monovalent group selected from alkyl, alkenyl, cycloalkyl, and aryl groups; ═NR 15 (to include triply bonded nitrogen (.tbd.N:) when R 15 is an electron pair and G is a single bond from at least one of Y 1 to Z 1 and Y 2 to Z 2 ); or --NR 18 R 19 in which R 18 and R 19 independently can be hydrogen, alkyl, cycloalkyl, aryl, a single bond, alkylene, cycloalkylene, or arylene, or together with the nitrogen atom to which they are joined form a ring of 4 to 12 ring atoms; G is --H; --NR 20 R 21 in which R 20 and R 21 independently are defined the same as R 11 , R 12 , and R 13 ; --NHR 20 ; --R 20 ; or --OR 20 ; ═O; polymeric monovalent and polyvalent groups; an electron pair; or a single bond; and q is an integer of 0 or greater and is equal to (the valence of G)-1.
Claim 5
Dependent Claim 118 words
The adduct according to claim 2 wherein X 1 and X 2 independently are --CH 2 ; --CH; --C; --CR 11 R 12 ; --CHR 11 ; --CR 11 ; --CW 1 W 2 ; --CR 11 W 1 ; --CHW 1 ; or --CW 1 ; in which R 11 , R 12 , W 1 and W 2 are as previously defined; Y 1 and Y 2 independently are doubly bonded oxygen (═O); doubly bonded sulfur (═S); ═CR 15 R 16 ; or ═NR 15 ; in which R 15 and R 16 are as previously defined; and Z 1 , Z 2 , G, q, p 1 , and p 2 are as previously defined.
Claim 6
Dependent Claim 89 words
The adduct according to claim 2 wherein X 1 and X 2 independently are --C, --CH, --CR 11 , or --CHR 11 in which R 11 is as previously defined; Z 1 and Z 2 are C; Y 1 and Y 2 independently are --CR 15 ═CR 16 R 17 or --NR 18 R 19 , in which R 15 , R 16 , R 17 , R 18 , and R 19 are as previously defined; and G, q, p 1 and p 2 are as previously defined.
Claim 7
Dependent Claim 71 words
The adduct according to claim 2 wherein X 1 and X 2 independently are --NW 1 in which W 1 is as previously defined; Z 1 and Z 2 independently are C; Y 1 and Y 2 independently are doubly bonded oxygen (═O); doubly bonded sulfur (═S); or ═NR 15 in which R 15 is as previously defined; and G, q, p 1 , and p 2 are as previously defined.
Claim 8
Dependent Claim 80 words
The adduct according to claim 2 wherein X 1 and X 2 independently are --NR 14 in which R 14 is as previously defined; Z 1 and Z 2 independently are C, N; Y 1 and Y 2 independently are doubly bonded oxygen (═O); doubly bonded sulfur (═S); ═CR 15 R 16 ; or ═NR 15 ; in which R 15 and R 16 are as previously defined; and G, q, p 1 and p 2 are as previously defined.
Claim 9
Dependent Claim 21 words
The adduct according to claim 2 wherein G contains one or more of S, O, N, P, halogen, and Si atoms.
Claim 10
Dependent Claim 46 words
The adduct according to claim 2 wherein G includes at least one functional group selected from the group consisting of alkyl, alkenyl, aryl, amide, thioamide, ester, thioester, ketone, thioketone, nitrile, nitro, sulfide, sulfoxide, disulfide, tertiary amine, ether, urethane, dithiocarbamate, quaternary ammonium, phosphonium, halogen, silyl, and silyloxy.
Claim 11
Dependent Claim 10 words
The adduct according to claim 2 wherein G is monovalent.
Claim 12
Dependent Claim 10 words
The adduct according to claim 2 wherein G is polyvalent.
Claim 13
Dependent Claim 13 words
The adduct according to claim 2 which is a precursor to an adhesive.
Claim 14
Dependent Claim 13 words
The adduct according to claim 2 which is a precursor to a sealant.
Claim 15
Dependent Claim 13 words
The adduct according to claim 2 which is a precursor to a coating.

References Cited (Backward Citations)

FR887530A Cited
US3694417A Cited
US4092298A Cited
US4291152A Cited
US4266040A Cited
US4485236A Cited
US4639286A Cited
US4785070A Cited

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