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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253669Generated: November 1, 2026

Acetyl chloride → Methyl-N-acetyl-1-methyl-2-(phenylmethylene)hydrazinecarboximidothioate

https://huagongshe.com/reaction/2253669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantMethyl-1-methyl-2-(phenylmethylene)hydrazinecarboximidothioate-hydroiodideHCID 70433894—
SolventDichloromethaneHCID 6344—
ProductMethyl-N-acetyl-1-methyl-2-(phenylmethylene)hydrazinecarboximidothioateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05232938
Source datasetuspto-grants-1993_08
ORD IDord-405d644f544b4767ab2ea47b264b90cb
Source noteuspto-grants-1993_08