GB1292383A - Process for production of acrylates and methacrylates of higher alcohols - Google Patents
Process for production of acrylates and methacrylates of higher alcoholsInfo
- Publication number
- GB1292383A GB1292383A GB637070A GB637070A GB1292383A GB 1292383 A GB1292383 A GB 1292383A GB 637070 A GB637070 A GB 637070A GB 637070 A GB637070 A GB 637070A GB 1292383 A GB1292383 A GB 1292383A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction
- acrylate
- methacrylate
- methacrylates
- acrylates
- 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
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/03—Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
- C07C67/52—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
- C07C67/54—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1292383 Transesterification UGILOR 10 Feb 1970 [25 Feb 1969] 6370/70 Heading C2C Acrylates or methacrylates are prepared by the reaction between an acrylate or methacrylate and a higher alcohol containing at least three carbon atoms at between 60‹ and 150‹ C. in the presence of a titanium phenoxide catalyst. The preferred catalyst is of general formula in which R 1 and R 2 each represents a hydrogen atom, alkyl (1-4 C), alkoxy (1-4 C), aryl, alkenyl (1-4 C), amino, alkylamino (1-4 C) or a phenylamino groups and R 3 , R 4 , and R 5 have the same meaning as R 1 and R 2 but also may be hydroxyl group. The higher alkanol may be linear a branched and primary or secondary and many are listed. The phenoxides may have a stabilizing effect on the reaction and may be prepared by reaction of phenol on titanium tetrachloride or transesterification of alkyl titanates with the phenol as solvent. Many phenols are specified. The lower ester is preferably ethyl or methyl, and examples describe the preparation of butyl methacrylate, and acrylate, 2-ethyl hexyl acrylate, and lauryl methacrylate using various phenoxide catalysts, the preparation of one of which, tetramethoxyphenyl titanate, being described.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR6904719A FR2033441A5 (en) | 1969-02-25 | 1969-02-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1292383A true GB1292383A (en) | 1972-10-11 |
Family
ID=9029538
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB637070A Expired GB1292383A (en) | 1969-02-25 | 1970-02-10 | Process for production of acrylates and methacrylates of higher alcohols |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE745581A (en) |
DE (1) | DE2008618A1 (en) |
FR (1) | FR2033441A5 (en) |
GB (1) | GB1292383A (en) |
LU (1) | LU60387A1 (en) |
NL (1) | NL7002443A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11174333B2 (en) | 2016-08-05 | 2021-11-16 | Basf Se | Macromonomers containing polyisobutene groups, and homopolymers or copolymers thereof |
WO2021257717A1 (en) * | 2020-06-19 | 2021-12-23 | Nitto Denko Corporation | Method for making bio-based acrylic acid |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5183930A (en) * | 1992-06-17 | 1993-02-02 | Rohm And Haas Company | Transesterification catalyst |
DE10127939A1 (en) | 2001-06-08 | 2002-05-29 | Basf Ag | Production of (meth)acrylate esters, e.g. dialkylaminoethyl (meth)acrylates, by catalytic transesterification involves four-stage distillation |
DE10127941A1 (en) | 2001-06-08 | 2002-05-29 | Basf Ag | Production of (meth)acrylate esters by transesterification comprises recycling by-product alcohol to the production of the starting (meth)acrylate |
DE10127938A1 (en) | 2001-06-08 | 2002-07-25 | Basf Ag | Production of basic dialkylaminoethyl(meth)acrylates, useful for production of (co)polymers for paints, dispersion or adhesives comprises esterification of (meth)acrylic acid alkyl esters. |
CN117729967A (en) | 2021-07-29 | 2024-03-19 | 巴斯夫欧洲公司 | Method for continuous distillation of acrylic ester |
-
1969
- 1969-02-25 FR FR6904719A patent/FR2033441A5/fr not_active Expired
-
1970
- 1970-02-06 BE BE745581D patent/BE745581A/en unknown
- 1970-02-10 GB GB637070A patent/GB1292383A/en not_active Expired
- 1970-02-20 NL NL7002443A patent/NL7002443A/xx unknown
- 1970-02-23 LU LU60387D patent/LU60387A1/xx unknown
- 1970-02-24 DE DE19702008618 patent/DE2008618A1/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11174333B2 (en) | 2016-08-05 | 2021-11-16 | Basf Se | Macromonomers containing polyisobutene groups, and homopolymers or copolymers thereof |
WO2021257717A1 (en) * | 2020-06-19 | 2021-12-23 | Nitto Denko Corporation | Method for making bio-based acrylic acid |
Also Published As
Publication number | Publication date |
---|---|
NL7002443A (en) | 1970-08-27 |
DE2008618A1 (en) | 1970-09-03 |
BE745581A (en) | 1970-07-16 |
LU60387A1 (en) | 1970-04-23 |
FR2033441A5 (en) | 1970-12-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed |