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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195661Generated: November 2, 2026

Chloroform → Benzyl 4-(3-ethoxy-3-oxopropyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1195661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
ReactantEthyl 3-piperidin-4-ylpropanoateHCID 10012639—
SolventWaterHCID 962—
ProductBenzyl 4-(3-ethoxy-3-oxopropyl)piperidine-1-carboxylateHCID 1498919174%

Reaction Steps

A mixture of 54 parts of (phenylmethyl)carbonochloridate, 60 parts of ethyl 4-piperidinepropanoate, 31.8 parts of sodium carbonate and 600 parts of trichloromethane was stirred overnight at room temperature. Water was added and the layers were separated. The organic layer was dried, filtered and evaporated. The residue was purified by filtration over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 71 parts (74%) of ethyl 1-(phenylmethoxycarbonyl)-4-piperidinepropanoate as a residue (interm. 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112825
Source datasetuspto-grants-1992_05
ORD IDord-08ff2416e8c942d3a0575bc504629310
Source noteuspto-grants-1992_05