Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489477Generated: October 30, 2026

Ethyl chloroformate → HCID 140376332, compound

https://huagongshe.com/reaction/1489477

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 added 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 numberUS05677448
Source datasetuspto-grants-1997_10
ORD IDord-a251f885e25d47319e7642cf897856e8
Source noteuspto-grants-1997_10