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Preparation of tertiary amines

Assignee: Honeywell UOP LLC
•
Filing: 1978-12-20
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Granted: 1981-02-10
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Expires: 1998-12-20
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Abstract

Abstract Tertiary amines may be prepared by reacting an olefinic compound, carbon monoxide, hydrogen and a nitrogen-containing compound such as ammonia, a primary amine or a secondary amine in the presence of a rhodium or ruthenium-containing catalyst at temperatures in the range of from about 50° to about 350° C. and a pressure in the range of from about 10 to about 300 atmospheres.

Inventors

  • 👤 Tamotsu Imai

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 19:30
CPC Classifications
C; C07; C07C; C07C209/00; C07C209/60; Y; Y02; Y02P; Y02P20/00; Y02P20/50; Y02P20/582

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 73 words
A process for the preparation of tertiary amines which comprises reacting an olefinic compound, carbon monoxide, hydrogen and a nitrogen-containing compound having the formula: ##STR3## in which the R's are independently selected from the group consisting of hydrogen, alkyl, aryl, cycloalkyl, aralykyl and alkaryl radicals in the presence of a rhodium catalyst selected from the group consisting of rhodium metal, nitrate, halides, chlorodicarbonylrhodium dimer and chlorobis(ethylene)rhodium dimer, and recovering the resultant tertiary amine.
Claim 2
Dependent Claim 73 words
A process for the preparation of tertiary amines which comprises reacting an olefinic compound, carbon monoxide, hydrogen and a nitrogen-containing compound having the formula: ##STR3## in which the R's are independently selected from the group consisting of hydrogen, alkyl, aryl, cycloalkyl, aralykyl and alkaryl radicals in the presence of a rhodium catalyst selected from the group consisting of rhodium metal, nitrate, halides, chlorodicarbonylrhodium dimer and chlorobis(ethylene)rhodium dimer, and recovering the resultant tertiary amine.
Claim 3
Dependent Claim 42 words
The process as set forth in claim 1 in which said reaction is effected at a temperature in the range of from about 50° to about 350° C. and a pressure in the range of from about 10 to about 300 atmospheres.
Claim 4
Dependent Claim 15 words
The process as set forth in claim 1 in which said catalyst is rhodium chloride.
Claim 5
Dependent Claim 15 words
The process as set forth in claim 1 in which said catalyst is chlorodicarbonylrhodium dimer.
Claim 6
Dependent Claim 15 words
The process as set forth in claim 1 in which said catalyst is chlorobis(ethylene)rhodium dimer.
Claim 7
Dependent Claim 25 words
The process as set forth in claim 1 in which said nitrogen-containing compound is dimethylamine, said olefin is undecene and said tertiary amine is dodecyldimethylamine.
Claim 8
Dependent Claim 25 words
The process as set forth in claim 1 in which said nitrogen-containing compound is dimethylamine, said olefin is heptene and said tertiary amine is octyldimethylamine.
Claim 9
Dependent Claim 25 words
The process as set forth in claim 1 in which said nitrogen-containing compound is aniline, said olefin is octene, and said tertiary amine is dinonylaniline.
Claim 10
Dependent Claim 25 words
The process as set forth in claim 1 in which said nitrogen-containing compound is ammonia, said olefin is pentene, and said tertiary amine is trihexylamine.
Claim 11
Dependent Claim 25 words
The process as set forth in claim 1 in which said nitrogen-containing compound is butylamine, said olefin is tetradecene, and said tertiary amine is di(pentadecyl)butylamine.

References Cited (Backward Citations)

US2422632A Cited
US2497310A Cited
US3574717A Cited
US3513200A Cited
US3758586A Cited
US4096150A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-02-10 1984-08-11 1985-02-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-02-10 1988-08-11 1989-02-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-02-10 1992-08-11 1993-02-10 $7700.00 Window Closed / Lapsed

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