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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426431Generated: October 30, 2026

Ethyl chloroformate → HCID 54202608, compound

https://huagongshe.com/reaction/426431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantSodiumHCID 5360545—
ReactantHCID 178503618HCID 178503618—
SolventAcetonitrileHCID 6342—
ProductHCID 54202608HCID 5420260886.9%

Reaction Steps

80.5 g of 2-(dimethylcarbamoylimino)-5-methylthio-1,3,4-thiadiazol-3-id, sodium salt, were suspended in 300 ml of acetonitrile and treated dropwise with stirring with 36.5 g of ethyl chloroformate at room temperature. The mixture was further stirred for 2 hours, treated with ice water, the precipitated substance separated by suction filtration, and recrystallized from acetonitrile. There is obtained 84.5 g (86.9% of theory) of 2-(dimethylcarbamoylimino)-5-methylthio-1,3,4-thiadiazolin-3-carboxylic acid ethyl ester of m. pt. 129° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04169718
Source datasetuspto-grants-1979_10
ORD IDord-717c82c94e04442897de762c40be3fbf
Source noteuspto-grants-1979_10