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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164601Generated: October 31, 2026

Ethyl chloroformate → 4-[2-(1-Ethoxycarbonyl-4-piperidyl)-ethyl]-2-phenyl quinoline

https://huagongshe.com/reaction/2164601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
Reactant2-Phenyl-4-(2-(4-piperidinyl)ethyl)quinolineHCID 71219—
SolventChloroformHCID 6212—
Product4-[2-(1-Ethoxycarbonyl-4-piperidyl)-ethyl]-2-phenyl quinolineHCID 12902716104.4%

Reaction Steps

A solution of 15.6 g of 2-phenyl-4-[2-(4-piperidyl)-ethyl]quinoline, prepared as indicated in Example 16, in 200 ml of chloroform is treated with stirring with 200 ml of a 1N aqueous solution of sodium hydroxide. Then 21.7 g of ethyl chloroformate are added, drop by drop, and the suspension obtained is stirred for 17 hours at the ambient temperature. After separation, the organic phase is washed with water, dried over magnesium sulphate, then evaporated under reduced pressure. 20 g of 4-[2-(1-ethoxycarbonyl-4-piperidyl)-ethyl]-2-phenyl-quinoline in the form of an oil are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04505916
Source datasetuspto-grants-1985_03
ORD IDord-ff04c08b5b7342ee88a1232240e7041a
Source noteuspto-grants-1985_03