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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129081Generated: October 30, 2026

1-Chloroethyl chloroformate → HCID 67783210, compound

https://huagongshe.com/reaction/129081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 53806431HCID 53806431—
SolventDichloromethaneHCID 6344—
ProductHCID 67783210HCID 6778321080.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

1.8 g of 1-chloroethyl chloroformate in 5 ml of methylene chloride are added dropwise to 2.9 g of 1-benzyl-3-(4-cyanobenzylidene)piperidine in 20 ml of methylene chloride at 0° C. and the mixture is stirred at 0° C. for 30 minutes. After 20 minutes at ambient temperature, it is evaporated down, the residue is taken up in 20 ml of methanol and the mixture is reflux-heated for 30 minutes. The reaction solution is evaporated down, and the residue is triturated with 100 ml of ethyl acetate and suction-filtered. 1.9 g of 3-(4-cyanobenzylidene)piperidine hydrochloride are obtained as a colourless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466687
Source datasetuspto-grants-1995_11
ORD IDord-28eed88fa1c548fa9b3ce634acfe479f
Source noteuspto-grants-1995_11