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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172274Generated: November 1, 2026

1-Chloroethyl chloroformate → HCID 68534030, compound

https://huagongshe.com/reaction/1172274

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantN-(1-benzylpiperidin-4-yl)naphthalene-1-carboxamideHCID 4064333—
SolventDichloromethaneHCID 6344—
ProductHCID 68534030HCID 6853403086.8%

Reaction Steps

A solution of N-(1-benzylpiperidin-4-yl)napth-1-yl carboxamide (1.38 g, 4.0 mmol) in dry CH2Cl2 (15 ml) was cooled to 0° C. and added α-chloroethyl chloroformate (1.14 g, 8.0 mmol) and stirred for 30 minutes. The mixture was evaporated in vacuo, added MeOH (15 ml) and heated under reflux for 1 h. The reaction mixture was evaporated in vacuo and the residue recrystallized from acetonitrile to give the product as a white powder (1.01 g, 86.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834010B2
Source datasetuspto-grants-2010_11
ORD IDord-704a08ebb6534118850f2d0f9bf7a3ce
Source noteuspto-grants-2010_11