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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418707Generated: October 25, 2026

Ethyl chloroformate → Carbamic acid, N-(cyanomethyl)-, ethyl ester

https://huagongshe.com/reaction/1418707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
ReactantAminoacetonitrile sulfate (1:1)HCID 196971—
SolventWaterHCID 962—
ProductCarbamic acid, N-(cyanomethyl)-, ethyl esterHCID 8370497%

Reaction Steps

Aminoacetonitrile sulfate (H2NCH2CN.1/2H2SO4, 121.5 g, 1.156mole) was dissolved in water (230.9 g) and the solution was cooled to 0° to 5° C. and adjusted to pH 5 to 7 by the addition of a small amount of 30% aqueous sodium hydroxide solution. Ethyl chloroformate (108.5 g, 1.00 mole) and 30% aqueous sodium hydroxide solution were concurrently added dropwise with stirring and keeping pH at 5 to 7 at 0° to 5° C. over 2 hours and the mixture was stirred at the same temperature for additional 2 hours while keeping the same pH by dropping, if necessary, 30% aqueous sodium hydroxide solution. The total amount of 30% aqueous sodium hydroxide solution was 294.3 g. The reaction mixture was extracted three times with toluene (485 ml). The toluene layer was dried over anhydrous magnesium sulfate, toluene was evaporated and the residue was cooled to room temperature to give crystals (124.7 g, 0.968 mole) of ethyl N-cyanomethylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883260
Source datasetuspto-grants-1999_03
ORD IDord-497022630c1f4e958d92caf3f54fefa2
Source noteuspto-grants-1999_03