HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorocyclohexanone → HCID 23312424, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorocyclohexanone | HCID 13203 | — |
| Reactant | 1-Formyl-3-thiosemicarbazide | HCID 2775486 | — |
| Reactant | HCID 23312414 | HCID 23312414 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23312424 | HCID 23312424 | — |
Reaction Steps
The 2-hydrazino-4,5,6,7-tetrahydro-benzothiazole hydrochloride used above is prepared in accordance with the method of Y.Usui [CA 70,96685 (1969)] via Hantzsch synthesis, with better yields by modification of the conditions. A mixture of 20 g of formylthiosemicarbazide, 22.3 g of 2-chlorocyclohexanone and 150 ml of dimethylformamide is kept at 70°-80° C. for 3 hours. On cooling, some of the product crystallises out. The dimethylformamide is distilled off in vacuo and the residue is recrystallised from ethanol. 27.4 g of 1-formyl-2-(4,5,6,7-tetrahydro-benzothiazolyl)-hydrazine hydrochloride of melting point 171°-173° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04600722 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-85e79c7c84a14e198a5d9b7ae9deefdc |
| Source note | uspto-grants-1986_07 |