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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248104Generated: October 25, 2026

Methyl chloroformate → methyl N-(2-phenylethanimidoyl)carbamate

https://huagongshe.com/reaction/1248104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Phenylethanimidamide hydrochlorideHCID 12415514—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Productmethyl N-(2-phenylethanimidoyl)carbamateHCID 14033885993%

Reaction Conditions

Temperature25 °C

Reaction Steps

137.2 parts of methyl chloroformate and a solution of 162.7 parts of potassium hydroxide in 180 parts of water are added via two inlets to a mixture of 246 parts of benzylmethanamidine hydrochloride in 530 parts of 1,2-dichloroethane and 85 parts of water, at from 10° to 15° C., in the course of 35 minutes. The mixture is stirred at 25° C. for 20 minutes, the organic phase is separated off and the aqueous phase is extracted twice more with 1,2- dichloroethane. The organic extracts are concentrated to give 259.8 parts (93% of theory) of N-methoxycarbonylbenzylmethanamidine of nD25 1.5247.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522763
Source datasetuspto-grants-1985_06
ORD IDord-57f5e323111041c28e2a20ddf672fbf6
Source noteuspto-grants-1985_06