HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Methyl-N-acetyl-1-methyl-2-(phenylmethylene)hydrazinecarboximidothioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl-1-methyl-2-(phenylmethylene)hydrazinecarboximidothioate-hydroiodide | HCID 70433894 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl-N-acetyl-1-methyl-2-(phenylmethylene)hydrazinecarboximidothioate | HCID 54432660 | — |
Reaction Steps
Methyl-1-methyl-2-(phenylmethylene)hydrazinecarboximidothioate-hydroiodide* (4 g) and triethylamine (2.5 g) were dissolved in dichloromethane (50 ml). To this solution acetyl chloride (1.05 g) was added slowly maintaining temperature below 20° C. The mixture was stirred at room temperature in a dry nitrogen atmosphere for 1.5 h. The organic residues were washed with water (5×20 ml), dried over anhydrous sodium sulphate and the solvent removed in vacuo giving a yellow solid which upon trituration with ether gave the title compound (2.30 g) as an off-white solid of m.pt. 102°-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05232938 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-405d644f544b4767ab2ea47b264b90cb |
| Source note | uspto-grants-1993_08 |