GB1267225A - - Google Patents
Info
- Publication number
- GB1267225A GB1267225A GB1267225DA GB1267225A GB 1267225 A GB1267225 A GB 1267225A GB 1267225D A GB1267225D A GB 1267225DA GB 1267225 A GB1267225 A GB 1267225A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali metal
- aug
- normal pressure
- reaction
- compound
- 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
- C07C67/04—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds
- C07C67/05—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds with oxidation
- C07C67/055—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds with oxidation in the presence of platinum group metals or their compounds
-
- 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
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
- B01J23/44—Palladium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/58—Platinum group metals with alkali- or alkaline earth metals
Abstract
1,267,225. Diacyloxyalkenes. FARBENFABRIKEN BAYER A.G. 4 Aug., 1970 [19 Aug., 1969; 29 Jan., 1970], No. 37520/70. Heading C2C. 1,3-Diacetoxy-2-methylene propane is prepared by passing isobutene, oxygen and acetic acid in the gas phase over a palladium-containing catalyst at 50‹ to 250‹ C. and at least some of the constituents boiling at temperatures above 150‹ C. at normal pressure, are removed from the reaction product whilst at least some of the constituents boiling at temperatures below 150‹ C. at normal pressure are recycled to the reaction. The catalyst may also contain at least one alkali metal acetate or alkali metal compound which under the reaction conditions is converted at least partly into an alkali metal acetate, and at least one metal or metal compound from the Vth to the VIIIth Group of the Periodic System and/or of gold and/or of copper, preferably an iron compound.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1942014A DE1942014C3 (en) | 1969-08-19 | 1969-08-19 | Process for the preparation of 13-diacetoxy-2-methylene propane |
DE19702003933 DE2003933A1 (en) | 1970-01-29 | 1970-01-29 | 1,3-diacetoxy 2-methylenepropane prepn |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1267225A true GB1267225A (en) | 1972-03-15 |
Family
ID=25757809
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1267225D Expired GB1267225A (en) | 1969-08-19 | 1970-08-04 |
Country Status (12)
Country | Link |
---|---|
JP (1) | JPS5412445B1 (en) |
BE (1) | BE755029A (en) |
BG (1) | BG21015A3 (en) |
CH (1) | CH539015A (en) |
FR (1) | FR2058981A5 (en) |
GB (1) | GB1267225A (en) |
HU (1) | HU162194B (en) |
LU (1) | LU61526A1 (en) |
NL (1) | NL152242B (en) |
PL (1) | PL80993B1 (en) |
SE (1) | SE7011262L (en) |
SU (1) | SU465780A3 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110891928A (en) * | 2017-07-24 | 2020-03-17 | 株式会社可乐丽 | Method for producing bisacyloylated exomethylene compound |
CN112299990A (en) * | 2020-11-11 | 2021-02-02 | 北京水木滨华科技有限公司 | Method and reaction system for preparing methyl allyl alcohol acetate through isobutene oxoacetylation |
CN112341314A (en) * | 2020-11-11 | 2021-02-09 | 北京水木滨华科技有限公司 | Method for preparing 2-methyl-1, 3-propylene glycol from isobutene |
CN112513001A (en) * | 2018-07-27 | 2021-03-16 | 株式会社可乐丽 | Method for producing 2-methyl-1-acyloxy-2-propene |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6110678B2 (en) * | 2012-02-10 | 2017-04-05 | 株式会社クラレ | Hydroxymethyl group-containing vinyl alcohol polymer |
-
0
- BE BE755029D patent/BE755029A/en unknown
-
1970
- 1970-07-20 CH CH1099370A patent/CH539015A/en not_active IP Right Cessation
- 1970-08-04 GB GB1267225D patent/GB1267225A/en not_active Expired
- 1970-08-10 SU SU1469811A patent/SU465780A3/en active
- 1970-08-14 BG BG1548070A patent/BG21015A3/xx unknown
- 1970-08-14 JP JP7084670A patent/JPS5412445B1/ja active Pending
- 1970-08-17 HU HUBA002460 patent/HU162194B/hu unknown
- 1970-08-17 LU LU61526D patent/LU61526A1/xx unknown
- 1970-08-18 PL PL14275570A patent/PL80993B1/pl unknown
- 1970-08-18 NL NL7012195A patent/NL152242B/en unknown
- 1970-08-18 SE SE7011262A patent/SE7011262L/sv unknown
- 1970-08-19 FR FR7030447A patent/FR2058981A5/fr not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110891928A (en) * | 2017-07-24 | 2020-03-17 | 株式会社可乐丽 | Method for producing bisacyloylated exomethylene compound |
CN112513001A (en) * | 2018-07-27 | 2021-03-16 | 株式会社可乐丽 | Method for producing 2-methyl-1-acyloxy-2-propene |
CN112299990A (en) * | 2020-11-11 | 2021-02-02 | 北京水木滨华科技有限公司 | Method and reaction system for preparing methyl allyl alcohol acetate through isobutene oxoacetylation |
CN112341314A (en) * | 2020-11-11 | 2021-02-09 | 北京水木滨华科技有限公司 | Method for preparing 2-methyl-1, 3-propylene glycol from isobutene |
CN112341314B (en) * | 2020-11-11 | 2021-11-02 | 北京水木滨华科技有限公司 | Method for preparing 2-methyl-1, 3-propylene glycol from isobutene |
Also Published As
Publication number | Publication date |
---|---|
JPS5412445B1 (en) | 1979-05-23 |
BG21015A3 (en) | 1976-01-20 |
SE7011262L (en) | 1971-02-22 |
SU465780A3 (en) | 1975-03-30 |
BE755029A (en) | 1971-02-19 |
NL152242B (en) | 1977-02-15 |
HU162194B (en) | 1973-01-29 |
NL7012195A (en) | 1971-02-23 |
CH539015A (en) | 1973-07-15 |
PL80993B1 (en) | 1975-08-30 |
FR2058981A5 (en) | 1971-05-28 |
LU61526A1 (en) | 1970-10-22 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |