GB766690A - 2-mercaptobenzothiazole derivatives and herbicidal compositions containing the same - Google Patents
2-mercaptobenzothiazole derivatives and herbicidal compositions containing the sameInfo
- Publication number
- GB766690A GB766690A GB17801/54A GB1780154A GB766690A GB 766690 A GB766690 A GB 766690A GB 17801/54 A GB17801/54 A GB 17801/54A GB 1780154 A GB1780154 A GB 1780154A GB 766690 A GB766690 A GB 766690A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzothiazylmercapto
- mercaptobenzthiazole
- benzthiazylmercapto
- dimer
- trichloroethylene
- 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
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/70—Sulfur atoms
- C07D277/74—Sulfur atoms substituted by carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention comprises (benzothiazylmercapto-2) pentachlorobutene, bis-(benzothiazylmercapto - 2) tetrachlorobutene, tris - (benzothiazylmercapto - 2) trichlorobutene, tetrakis(benzothiazylmercapto - 2) dichlorobutene, pentakis - (benzothiazylmercapto - 2) chlorobutene and hexakis-(benzothiazylmercapto-2) butene and mixtures thereof, and their preparation by reacting 2-mercaptobenzthiazole or an alkali metal derivative thereof with dimeric trichloroethylene. The reaction may be effected by mixing the reactants and allowing the mixture to stand, or by refluxing in an inert solvent, e.g. toluene, ethanol, nitrobenzene or ether. Alkali metal mercaptides mentioned are those of lithium sodium and potassium. In examples (1) 2-mercaptobenzthiazole is treated with ethanolic sodium hydroxide, the mixture filtered, cooled and dimeric trichloroethylene added; after leaving overnight mixture is filtered, and filtrate on standing for a month deposits a condensate of 2-mercaptobenzthiazole and trichloroethylene-dimer; (2) a suspension of sodium mercaptobenzthiazole in ether is treated with dimeric trichloroethylene as in (1); (3) as in (1), but refluxing the reaction mixture, to yield a condensation product in which substantially all the chlorine of the dimer is replaced; (4) mercaptobenzthiazole and the dimer are refluxed in toluene, giving essentially a mono - (benzothiazylmercapto - 2) pentachlorobutene; (5) ethanolic sodium mercaptobenzthiazole and the dimer are refluxed in toluene, and the condensation product obtained crystallized from alcohol.ALSO:Herbicidal compositions comprise the reaction product obtained by condensing 2-mercaptobenzthiazole or an alkali metal derivative thereof with trichoroethylene dimer, (i.e. (benzthiazylmercapto-2)- pentachlorobutene, bis (benzthiazylmercapto-2) tetrachlorobutene, tris (benzthiazylmercapto-2) trichlorobutene, tetrakis (benzthiazytmercapto-2) dichlorobutene, pentakis (benzthiazylmercapto-2) chlorobutene, hexakis (benzthiazylmercapto-2)-butene and mixtures thereof), and a finely-divided solid or a liquid carrier. Oil-in-water emulsions of the active compounds (cyclohexanone is the preferred organic medium), in corporate ionic or non-ionic emulsifying agents, e.g. alkylbenzene sulphonates and polyglycol ethers, and may further include other agricultural pesticides, insecticides and fungicides. Specified solid carriers are clay, pumice, talc and bentonite.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US766690XA | 1953-06-17 | 1953-06-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB766690A true GB766690A (en) | 1957-01-23 |
Family
ID=22133486
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB17801/54A Expired GB766690A (en) | 1953-06-17 | 1954-06-17 | 2-mercaptobenzothiazole derivatives and herbicidal compositions containing the same |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB766690A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0420453A1 (en) * | 1989-09-27 | 1991-04-03 | Mobil Oil Corporation | Sulphur coupled hydrocarbyl derived mercaptobenzothiazole adducts as multifunctional antiwear additives and compositions containing same |
-
1954
- 1954-06-17 GB GB17801/54A patent/GB766690A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0420453A1 (en) * | 1989-09-27 | 1991-04-03 | Mobil Oil Corporation | Sulphur coupled hydrocarbyl derived mercaptobenzothiazole adducts as multifunctional antiwear additives and compositions containing same |
US5073279A (en) * | 1989-09-27 | 1991-12-17 | Mobil Oil Corporation | Sulfur coupled hydrocarbyl derived mercaptobenzothiazole adducts as multifunctional antiwear additives and compositions containing same |
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