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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112291Generated: October 26, 2026

Methyl chloroformate → N-carbomethoxy-O-methylisourea

https://huagongshe.com/reaction/1112291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantSodium HydroxideHCID 14798—
ReactantCarbamimidic acid, methyl ester, sulfate (1:1)HCID 169039—
SolventWaterHCID 962—
ProductN-carbomethoxy-O-methylisoureaHCID 53429793—

Reaction Steps

To 52 parts of 2-methylpseudourea hydrogen sulfate in 250 parts of water at 0°-5° C. is added 31 parts of methyl chloroformate followed by dropwise addition of 74 parts of 50% sodium hydroxide. The reaction mass is stirred at room temperature for 3 hours and then extracted with methylene chloride. The methylene chloride extract is dried and the solvent evaporated. The residue is triturated with hexane to give 23 parts of methyl N-(1-amino-1-methoxy methylene)carbamate melting at 36°-39.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04121921
Source datasetuspto-grants-1978_10
ORD IDord-c620b4aa2cb441edb5857353f5d62d2e
Source noteuspto-grants-1978_10