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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645484Generated: October 29, 2026

1-Chloroethyl chloroformate → HCID 68708639, compound

https://huagongshe.com/reaction/645484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 68708945HCID 68708945—
SolventDichloromethaneHCID 6344—
ProductHCID 68708639HCID 68708639—

Reaction Steps

To a solution of [1-(4-methoxy-benzyl)-4-phenylpiperidin-4-ylmethyl]carbamic acid tert-butyl ester (3.2 mmol) in CH2Cl2 is added 1-chloroethyl chloroformate (4.7 mmol), then the mixture is stirred at room temperature for 2.5 h. After the bulk of solvent is concentrated in vacuo, the residue suspended in ether and filtered. After the filtrate is concentrated in vacuo, the residue is suspended in hexane and filtered. The filtrate is concentrated in vacuo to give the 4-(tert-butoxycarbonylaminomethyl)-4-phenylpiperidine-1-carboxylic acid 1-chloroethyl ester, which is directly used for the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704996B2
Source datasetuspto-grants-2010_04
ORD IDord-72f8b51875a340da94a028b88605c3f6
Source noteuspto-grants-2010_04