Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963848Generated: October 31, 2026

Ethyl chloroformate → HCID 140376332, compound

https://huagongshe.com/reaction/963848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86748617HCID 86748617—
SolventDichloromethaneHCID 6344—
ProductHCID 140376332HCID 140376332—

Reaction Steps

0.55 ml of ethyl chloroformate is addled dropwise to a solution of 2.0 g of benzyl [[(S)-1-amidino-3-piperidinyl]methyl]carbamate hydrochloride in 200 ml of methylene chloride. The reaction mixture is cooled to 0°. 113 ml of 0.1N sodium hydroxide solution are added dropwise while stirring. Subsequently, the mixture is stirred in an ice bath. The phases are separated. The organic phase is washed with water, dried and evaporated. There are obtained 1.5 g of benzyl (S)-1-(ethoxycarbonylamino-imino-methyl)-piperidin-3-ylmethylcarbamate, MS (FAB): 363.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763604
Source datasetuspto-grants-1998_06
ORD IDord-ec66a34b69364d8696696d442ef83e13
Source noteuspto-grants-1998_06