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US4310704A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for manufacturing methyl ketones by oxidation of terminal olefins

Assignee: IFP Energies nouvelles
•
Filing: 1979-12-18
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Granted: 1982-01-12
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Expires: 1999-12-18
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Abstract

Abstract Methyl ketones are prepared in liquid phase by oxidizing terminal olefins of the formula R-CH=CH2, where R is a hydrocarbon radical. The oxidizing agent is hydrogen peroxide or an organic hydroperoxide, and the catalyst is a palladium catalyst of the formula Pd AA', (Lm) where A is fluoborate, acetate or trefrafluoroacetate A' is the same as A or is pi -allyl, m is 0 or 2, and L is a ligand selected from the amines, the phosphines, the arsines, the stibines and the amides.

Inventors

  • 👤 Hubert Mimoun
  • 👤 Robert Charpentier
  • 👤 Michel Roussel

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 18:24
CPC Classifications
C; C07; C07C; C07C45/00; C07C45/27; C07C45/28

Claims Analysis

Total Claims: 21
Claim 1
Independent Claim 129 words
A process for producing a methyl ketone of the formula ##STR2## from an olefin of the formula CH 2 ═CHR wherein R is C 1-20 hydrocarbyl, said process comprising the step consisting essentially of contacting said olefin in the liquid phase, optionally in the presence of a solvent, with a palladium catalyst and a peroxide oxidizing agent; wherein said palladium catalyst has the formula PdAA'(L) m , wherein A is fluoborate, acetate or trifluoroacetate; A' is the same as A or a π-allyl radical; L is an amine, phosphine, arsine, stibine or amide ligand; and m is 0 or 2; and wherein said oxidizing agent is hydrogen peroxide or an organic hydroperoxide of the formula R 2 OOH, wherein R 2 is C 4-20 tertiary alkyl, aralkyl or alkylaryl.
Claim 2
Dependent Claim 129 words
A process for producing a methyl ketone of the formula ##STR2## from an olefin of the formula CH 2 ═CHR wherein R is C 1-20 hydrocarbyl, said process comprising the step consisting essentially of contacting said olefin in the liquid phase, optionally in the presence of a solvent, with a palladium catalyst and a peroxide oxidizing agent; wherein said palladium catalyst has the formula PdAA'(L) m , wherein A is fluoborate, acetate or trifluoroacetate; A' is the same as A or a π-allyl radical; L is an amine, phosphine, arsine, stibine or amide ligand; and m is 0 or 2; and wherein said oxidizing agent is hydrogen peroxide or an organic hydroperoxide of the formula R 2 OOH, wherein R 2 is C 4-20 tertiary alkyl, aralkyl or alkylaryl.
Claim 3
Dependent Claim 101 words
A process according to claim 1, wherein the catalyst is one of palladium acetate, palladium trifluoracetate, palladium fluoborate or a complex of the formula: Pd(CH 3 CO 2 ) 2 [P(C 6 H 5 ) 3 ] 2 (CF 3 CO 2 ) 2 Pd[P(C 6 H 5 ) 3 ] 2 CF 3 CO 2 Pd--O--O--C(CH 3 ) 3 CH 3 CO 2 Pd--O--O--C(CH 3 ) 3 Pd(CH 3 CO 2 ) 2 (HMPT) 2 Pd(CF 3 CO 2 ) 2 (HMPT) 2 (CH 3 CO 2 )Pd-π-C 6 H 11 (CF 3 CO 2 )Pd-π-C 6 H 11 .
Claim 4
Dependent Claim 37 words
A process according to claim 2, wherein said oxidizing agent is hydrogen peroxide, the molar ratio H 2 O 2 /olefin being from 0.1 to 10, and the ratio by weight olefin/catalyst being from 10 to 10,000.
Claim 5
Dependent Claim 30 words
A process according to claim 3, wherein the molar ratio H 2 O 2 /olefin is from 1.5 to 5, the ratio by weight olefin/catalyst being from 100 to 1,000.
Claim 6
Dependent Claim 14 words
A process according to claim 4, wherein hydrogen peroxide is used in aqueous solution.
Claim 7
Dependent Claim 33 words
A process according to claim 5, wherein the olefin is further diluted in an organic solvent, said solvent being a chlorinated hydrocarbon, an ester, an aromatic solvent, an alcohol, or a monocarboxylic acid.
Claim 8
Dependent Claim 18 words
A process according to claim 6, wherein the solvent is chloroform, ethyl acetate, tert-butyl alcohol, or acetic acid.
Claim 9
Dependent Claim 30 words
A process according to claim 4, wherein the hydrogen peroxide and the olefin are dissolved in an organic solvent, said solvent being an alcohol, a cyclic ether, or an amide.
Claim 10
Dependent Claim 34 words
A process according to claim 2, wherein said oxidizing agent is tert-butyl or cumyl hydroperoxide, the molar ratio olefin/hydroperoxide being from 0.1 to 10 and the molar ratio olefin/catalyst being from 10 to 10,000.
Claim 11
Dependent Claim 25 words
A process according to claim 9, wherein the molar ratio olefin/hydroperoxide is from 0.1 to 0.5, the molar ratio olefin/catalyst being from 100 to 1,000.
Claim 12
Dependent Claim 26 words
A process according to claim 1, wherein in said catalyst, the π-allyl radical is a 1-methyl-3-ethyl-π-allyl radical; and L is one of triphenylphosphine, dimethylformamide and hexamethylphosphoramide.
Claim 13
Dependent Claim 17 words
A process according to claim 1, wherein said step is effected in the absence of chloride ions.
Claim 14
Dependent Claim 85 words
A process according to claim 1, wherein the catalyst is one of palladium acetate, palladium trifluoroacetate palladium fluoborate or a complex of the formula: Pd(CH 3 CO 2 ) 2 [P(C 6 H 5 ) 3 ] 2 (CF 3 CO 2 ) 2 Pd[P(C 6 H 5 ) 3 ] 2 Pd(CH 3 CO 2 ) 2 (HMPT) 2 Pd(CF 3 CO 2 ) 2 (HMPT) 2 (CH 3 CO 2 )Pd-π-C 6 H 11 (CF 3 CO 2 )Pd-π-C 6 H 11 .
Claim 15
Dependent Claim 20 words
A process according to claim 3, wherein said step is effected at a temperature of from 0° to 130° C.
Claim 16
Dependent Claim 20 words
A process according to claim 4, wherein said step is effected at a temperature of from 40° to 70° C.
Claim 17
Dependent Claim 20 words
A process according to claim 8, wherein said organic solvent is methanol, ethanol, isopropanol, tert.-butanol, tetrahydrofuran dioxane, dimethylformamide, or hexamethylphosphoramide.
Claim 18
Dependent Claim 20 words
A process according to claim 9, wherein said step is effected at a temperature of from 0° to 120° C.
Claim 19
Dependent Claim 20 words
A process according to claim 10, wherein said step is effected at a temperature of from 20° to 80° C.
Claim 20
Dependent Claim 30 words
A process according to claim 10, wherein said step is effected in the presence of a solvent, said solvent being a chlorinated hydrocarbon, an aromatic solvent, or a nitrogen-containing solvent.
Claim 21
Dependent Claim 18 words
A process according to claim 19, wherein said solvent is dichloroethane, chlorobenzene, dichlorobenzene, benzene, toluene, xylene, or nitrobenzene.

References Cited (Backward Citations)

US3122586A Cited
US3231620A Cited
US3370073A Cited
US3318891A Cited
US3410807A Cited
US3932521A Cited
US3927111A Cited
US3879467A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-01-11 1985-07-13 1986-01-12 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-01-11 1989-07-13 1990-01-12 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-01-11 1993-07-13 1994-01-12 $7700.00 Window Closed / Lapsed

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