GB747048A - Improvements in the production of 2.5-dimercapto-1.3.4- thiadiazole - Google Patents
Improvements in the production of 2.5-dimercapto-1.3.4- thiadiazoleInfo
- Publication number
- GB747048A GB747048A GB6193/54A GB619354A GB747048A GB 747048 A GB747048 A GB 747048A GB 6193/54 A GB6193/54 A GB 6193/54A GB 619354 A GB619354 A GB 619354A GB 747048 A GB747048 A GB 747048A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali
- dimercapto
- hydrazine
- reaction
- solution
- 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
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
2,5 - Dimercapto - 1,3,4 - thiodiazole is prepared by reacting about 2 mols. of carbon disulphide with about 1 mol. of hydrazine at elevated temperature and in the presence of at least three equivalents of caustic soda solution, followed by acidifying the resultant solution (e.g. with hydrochloric acid). Strongly alkaline technical solutions of hydrazine can be employed, e.g. those obtained from the reaction of ammonia and alkali-hypochlorite solutions, or from urea, alkali-hypochlorite and caustic alkali solution. The reaction is preferably conducted at 50 DEG to 80 DEG C., and in presence of solvents (e.g. alcohols or ethers) and/or emulsifiers.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE747048X | 1953-03-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB747048A true GB747048A (en) | 1956-03-28 |
Family
ID=6648541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6193/54A Expired GB747048A (en) | 1953-03-14 | 1954-03-03 | Improvements in the production of 2.5-dimercapto-1.3.4- thiadiazole |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB747048A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109912536A (en) * | 2019-03-18 | 2019-06-21 | 山东昌邑四方医药化工有限公司 | A kind of dimercapto -1,3,4 2,5-, the synthetic method of-thiadiazoles |
RU2743164C1 (en) * | 2020-04-24 | 2021-02-15 | Общество с ограниченной ответственностью Научно-производственное предприятие "КФ" | Method for the preparation of 2,5-dimercapto-1,3,4-thiadiazole (dmtd) |
-
1954
- 1954-03-03 GB GB6193/54A patent/GB747048A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109912536A (en) * | 2019-03-18 | 2019-06-21 | 山东昌邑四方医药化工有限公司 | A kind of dimercapto -1,3,4 2,5-, the synthetic method of-thiadiazoles |
RU2743164C1 (en) * | 2020-04-24 | 2021-02-15 | Общество с ограниченной ответственностью Научно-производственное предприятие "КФ" | Method for the preparation of 2,5-dimercapto-1,3,4-thiadiazole (dmtd) |
WO2021215958A1 (en) * | 2020-04-24 | 2021-10-28 | Общество с ограниченной ответственностью Научно-производственное предприятие "КФ" | Method for producing 2,5-dimercapto-1,3,4-thiadiazole (dmtd) and 2,5-dimercapto-1,3,4-thiadiazole produced by said method |
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