GB1140514A - Process for the production of 2-acylimino-1,3-oxathiolanes - Google Patents
Process for the production of 2-acylimino-1,3-oxathiolanesInfo
- Publication number
- GB1140514A GB1140514A GB2125466A GB2125466A GB1140514A GB 1140514 A GB1140514 A GB 1140514A GB 2125466 A GB2125466 A GB 2125466A GB 2125466 A GB2125466 A GB 2125466A GB 1140514 A GB1140514 A GB 1140514A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxathiolanes
- acylimino
- benzoylimino
- oxathiolane
- phenoxymethyl
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
- C07D327/04—Five-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,140,514. Acylimino-oxathiolanes. CHEMISCHE WERKE HULS A.G. 13 May, 1966 [15 May, 1965], No. 21254/66. Heading C2C. 2 - Acylimino - 1,3 - oxathiolanes are prepared by reacting a N-dichloromethylene amide of the formula where R represents C 1-6 alkyl or cycloalkyl group or an aryl group which may be substituted by nitro, halogeno or akloxy groups, with a monothioglycol of the formula where R<SP>1</SP> and R<SP>2</SP> are C 1-6 alkyl, cycloalkyl radicals or an aryl radical optionally substituted by alkoxy or aryloxy groups, at 0-50‹ C. in the presence of an inert solvent and a tertiary amine. It is preferred to effect the reaction at 0-10‹ C. using equimolar proportions of reactants and 10-80% by weight tertiary amine, based on reaction mixture. Examples describe the preparation of 2-benzoylimino-5- phenoxymethyl - 1,3 - oxathiolane, 2 - benzoylimino - 4 - phenoxymethyl - 1,3 - oxathiolane and 2-benzoylimino-5-methyl-1,3-oxathiolane.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEC35861A DE1242631B (en) | 1965-05-15 | 1965-05-15 | Process for the preparation of 2-acylimino-1-oxa-3-thiacyclopentanes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1140514A true GB1140514A (en) | 1969-01-22 |
Family
ID=7022015
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2125466A Expired GB1140514A (en) | 1965-05-15 | 1966-05-13 | Process for the production of 2-acylimino-1,3-oxathiolanes |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1242631B (en) |
GB (1) | GB1140514A (en) |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE632578A (en) * | 1963-05-22 |
-
1965
- 1965-05-15 DE DEC35861A patent/DE1242631B/en active Pending
-
1966
- 1966-05-13 GB GB2125466A patent/GB1140514A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE1242631B (en) | 1967-06-22 |
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