GB760643A - Preparation of dithiocarbamic acid derivatives - Google Patents
Preparation of dithiocarbamic acid derivativesInfo
- Publication number
- GB760643A GB760643A GB2180157A GB2180157A GB760643A GB 760643 A GB760643 A GB 760643A GB 2180157 A GB2180157 A GB 2180157A GB 2180157 A GB2180157 A GB 2180157A GB 760643 A GB760643 A GB 760643A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- thiazole
- formula
- mercaptide
- thiazoline
- 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)
- Thiazole And Isothizaole Compounds (AREA)
Abstract
Dithiocarbamates of the formula <FORM:0760643/IV(b)/1> where R1 is alkyl, aralkyl or aryl, R2 is alkyl or aralkyl (or R1, R2 together form a polymethylene or oxapolymethylene chain), and Q completes a thiazole, thiazoline or arylene-thiazole ring are prepared by reacting thiophosgene in the presence of water with an amine HNR1R2, a mercaptide of the formula <FORM:0760643/IV(b)/2> where M is an alkali or alkaline earth metal, and an inorganic basic alkali or alkaline earth metal compound; the last three are present during the reaction in at least a stoichiometric amount with respect to the thiophosgene. Preferably the latter is introduced into an agitated aqueous mixture of the other reactants, the temperature being maintained below 100 DEG C. e.g. at 10-40 DEG C. An organic solvent may also be present if desired. The mercaptide of the above formula may be derived from thiazole, alkylthiazoles, thiazoline, alkylthiazolines, benzthiazole or naphthothiazole, the latter being optionally ring-substituted by halogen, alkyl or nitro groups. Many suitable groups are mentioned for Q, R1 and R2. The metal M may be sodium, potassium, calcium, strontium, barium or magnesium. An example is given of the production of benzthiazol-2-yl-N:N-diethyldithiocarbamate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2180157A GB760643A (en) | 1954-07-26 | 1954-07-26 | Preparation of dithiocarbamic acid derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2180157A GB760643A (en) | 1954-07-26 | 1954-07-26 | Preparation of dithiocarbamic acid derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB760643A true GB760643A (en) | 1956-11-07 |
Family
ID=10169039
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2180157A Expired GB760643A (en) | 1954-07-26 | 1954-07-26 | Preparation of dithiocarbamic acid derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB760643A (en) |
-
1954
- 1954-07-26 GB GB2180157A patent/GB760643A/en not_active Expired
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