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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464781Generated: October 25, 2026

Methyl chloroformate → HCID 86740383, compound

https://huagongshe.com/reaction/464781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl beta-amino-beta-ethoxyacrylate hydrochlorideHCID 53395434—
SolventDichloromethaneHCID 6344—
ProductHCID 86740383HCID 86740383—

Reaction Steps

A solution consisting of 96 g of ethyl β-amino-β-ethoxyacrylate hydrochloride, 800 ml of methylene chloride and 120 ml of N-methylmorpholine is warmed to 40°. While stirring there is added dropwise within 2 hours a solution of 65 ml of methyl chloroformate in 350 ml of methylene chloride. After completion of the addition, the mixture is stirred at 40° for a further 2 hours. Thereupon, the resulting salt is filtered off under suction and washed with about 50 ml of methylene chloride. The filtrate is evaporated at 40° in a water-jet vacuum. There is obtained crude methyl[(1-ethoxy-2-ethoxycarbonyl)-ethylidene]carbamate in the form of a pale yellow oil which is used immediately in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04549019
Source datasetuspto-grants-1985_10
ORD IDord-9784dfae229a4f8299c9b1e165277e01
Source noteuspto-grants-1985_10