GB490571A - Improvements in or relating to the manufacture of halogen derivatives of aceto propyl alcohol - Google Patents
Improvements in or relating to the manufacture of halogen derivatives of aceto propyl alcoholInfo
- Publication number
- GB490571A GB490571A GB23743/37A GB2374337A GB490571A GB 490571 A GB490571 A GB 490571A GB 23743/37 A GB23743/37 A GB 23743/37A GB 2374337 A GB2374337 A GB 2374337A GB 490571 A GB490571 A GB 490571A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aceto
- butyrolactone
- halogen
- relating
- manufacture
- 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
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/04—Saturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/17—Saturated compounds containing keto groups bound to acyclic carbon atoms containing hydroxy groups
- C07C49/173—Saturated compounds containing keto groups bound to acyclic carbon atoms containing hydroxy groups containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/673—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Halogen compounds are prepared by chlorinating or brominating a -aceto-g -butyrolactone, and if desired, hydrolysing the product with dilute acid. Chlorine, sulphuryl chloride or bromine are used for the halogenation, whilst the hydrolysis is preferably effected by the acid of the halogen previously used. The final products are halogen derivatives of acetopropyl alcohol which are useful as intermediates in the synthesis of Vitamin B1, e.g. by the process described in Specification 472,459. Examples are given. a -Aceto-g -butyrolactone is obtained by reacting ethyl acetoacetate with ethylene oxide. The Specification as open to inspection under Sect. 91 also describes the halogenation of the alkyl derivatives of a - aceto-g -butyrolactone and refers to sulphuryl bromide as a brominating agent. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US490571XA | 1936-09-01 | 1936-09-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB490571A true GB490571A (en) | 1938-08-17 |
Family
ID=21957836
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23743/37A Expired GB490571A (en) | 1936-09-01 | 1937-08-31 | Improvements in or relating to the manufacture of halogen derivatives of aceto propyl alcohol |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB490571A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111072465A (en) * | 2019-12-27 | 2020-04-28 | 江苏兄弟维生素有限公司 | Esterification hydrolysis process, esterification hydrolysis reactor and application |
-
1937
- 1937-08-31 GB GB23743/37A patent/GB490571A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111072465A (en) * | 2019-12-27 | 2020-04-28 | 江苏兄弟维生素有限公司 | Esterification hydrolysis process, esterification hydrolysis reactor and application |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB404938A (en) | Manufacture of chlorhydrins and ethers thereof | |
GB1325275A (en) | 1-chloro-2,2,3,3-tetrafluoropropyl difluoromethyl ether | |
GB490571A (en) | Improvements in or relating to the manufacture of halogen derivatives of aceto propyl alcohol | |
US2193858A (en) | Halogenated organic compounds | |
GB341926A (en) | Process for the manufacture of homogeneous halogen derivatives of ª-chloro-naphthalene | |
US2223885A (en) | Halogenated derivatives of | |
GB462693A (en) | Process for the manufacture of new acid wool dyestuffs of the anthraquinone series | |
GB349455A (en) | Improvements relating to barbituric acid derivatives | |
GB489612A (en) | Manufacture of fluorene derivatives | |
GB454400A (en) | A process of producing carboxylic saturated and/or unsaturated acids, their salts and/or their ketol-esters | |
GB770593A (en) | Chlorinated hydroxyindanes | |
GB399769A (en) | Manufacture of 6-bromo (or -chloro)-2:4-dinitraniline | |
GB336495A (en) | ||
GB432955A (en) | Improvements in or relating to the preparation of halogen phenols | |
GB460911A (en) | Manufacture of 3:4:5:6-halogen-2-amino-1-oxybenzenes | |
GB647094A (en) | Improvements in and relating to the manufacture of isovaleric acid | |
GB263845A (en) | Manufacture of benzanthrone derivatives | |
GB440822A (en) | Improvements in the manufacture and production of vat dyestuffs | |
GB473923A (en) | Improvements in or relating to preparation of sterol derivatives | |
GB473470A (en) | Improvements in or relating to the hydrolysis of titanium salt solutions | |
GB396251A (en) | Improvements in or relating to derivatives of 2-hydroxy-diphenyl | |
GB445206A (en) | Improvements in and relating to the production of chlorinated compounds of isopropyl amine | |
GB467482A (en) | The manufacture of unsaturated diketones related to the corpus luteum hormone | |
GB455991A (en) | Process for the manufacture of a chrysene monosulphonic acid | |
GB969286A (en) | Process for the production of basic thymyl ethers |