GB987274A - Improvements in and relating to the production of halides of unsaturated aliphatic acids or derivatives thereof - Google Patents
Improvements in and relating to the production of halides of unsaturated aliphatic acids or derivatives thereofInfo
- Publication number
- GB987274A GB987274A GB3350262A GB3350262A GB987274A GB 987274 A GB987274 A GB 987274A GB 3350262 A GB3350262 A GB 3350262A GB 3350262 A GB3350262 A GB 3350262A GB 987274 A GB987274 A GB 987274A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloride
- chlorobut
- ene
- palladium
- halides
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Halides of unsaturated aliphatic carboxylic acids are prepared by contacting a compound containing the grouping <FORM:0987274/C2/1> wherein X is a halogen atom and the free valencies indicated are attached to hydrogen atoms or alkyl groups, with carbon monoxide in the presence of palladium or a complex or a salt thereof at a temperature of at most 250 DEG C. and at a pressure of at most 3000 atmospheres. The acid halides may be reacted subsequently with water, an alcohol, ammonia or an amine to give, respectively, the corresponding acid, ester or unsubstituted or substituted amide. In a modification of the process the acid, ester or amide is produced directly by conducting the carbonylation reaction as above in the presence of water, an alcohol, ammonia or an amine. Specified catalysts are metallic palladium, palladous chloride, p -allyl palladium chloride, p -methallyl palladium chloride and p -crotyl palladium chloride. Examples are given. The following conversions of starting materials also occur in the examples:-(6) 1-chlorobut-2-ene to 3 - chlorobut - 1 - ene; (7) 3 - chlorobut - 1 - ene to 1-chlorobut-2-ene; (8) methallyl chloride to tertiary-butyl chloride.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3350262A GB987274A (en) | 1962-08-31 | 1962-08-31 | Improvements in and relating to the production of halides of unsaturated aliphatic acids or derivatives thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3350262A GB987274A (en) | 1962-08-31 | 1962-08-31 | Improvements in and relating to the production of halides of unsaturated aliphatic acids or derivatives thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
GB987274A true GB987274A (en) | 1965-03-24 |
Family
ID=10353794
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3350262A Expired GB987274A (en) | 1962-08-31 | 1962-08-31 | Improvements in and relating to the production of halides of unsaturated aliphatic acids or derivatives thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB987274A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2606773A1 (en) * | 1986-11-14 | 1988-05-20 | Rhone Poulenc Chimie | PROCESS FOR THE PREPARATION OF HEXENEDIOIC ACID DIESTERS |
EP0640580A1 (en) * | 1993-07-26 | 1995-03-01 | E.I. Du Pont De Nemours And Company | Preparation of 3-pentenoic acid and a catalyst therefore |
US5399753A (en) * | 1994-05-04 | 1995-03-21 | Dsm, N. V. | Catalyst recovery in the carbonylation of chlorobutenes to pentenoyl chloride |
WO1997029069A1 (en) * | 1996-02-12 | 1997-08-14 | Dsm N.V. | Process for the preparation of pentenoic acid or pentenoate ester |
-
1962
- 1962-08-31 GB GB3350262A patent/GB987274A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2606773A1 (en) * | 1986-11-14 | 1988-05-20 | Rhone Poulenc Chimie | PROCESS FOR THE PREPARATION OF HEXENEDIOIC ACID DIESTERS |
EP0272191A1 (en) * | 1986-11-14 | 1988-06-22 | Rhone-Poulenc Chimie | Process for the preparation of diesters of hexenedioic acid |
US4857657A (en) * | 1986-11-14 | 1989-08-15 | Rhone-Poulenc Chimie | Preparation of hexenedioic acid diesters |
EP0640580A1 (en) * | 1993-07-26 | 1995-03-01 | E.I. Du Pont De Nemours And Company | Preparation of 3-pentenoic acid and a catalyst therefore |
US5399753A (en) * | 1994-05-04 | 1995-03-21 | Dsm, N. V. | Catalyst recovery in the carbonylation of chlorobutenes to pentenoyl chloride |
WO1997029069A1 (en) * | 1996-02-12 | 1997-08-14 | Dsm N.V. | Process for the preparation of pentenoic acid or pentenoate ester |
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