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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004962Generated: October 31, 2026

HCID 22126486, compound → HCID 22128104, compound

https://huagongshe.com/reaction/1004962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22126486HCID 22126486—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 22128104HCID 2212810474.6%

Reaction Steps

A suspension of 0.420 g (0.8 mmol) of 2,2,2-trichloroethyl 4-(4-chloro-phenyl)-3-(naphthalen-2-ylmethoxy)-piperidine-1-carboxylate and 300 mg of zinc in 10 ml of acetic acid was stirred at room temperature for 12 hours. The reaction solution was diluted with 40 ml of water and extracted four times with 30 ml of methylene chloride. The organic phase was washed twice with 40 ml of 1N sodium hydroxide solution each time, dried over sodium sulphate, filtered and evaporated. The residue was chromatographed on silica gel using a 9:1 mixture of methylene chloride and methanol as the eluent. There was obtained 0.210 g (74% of theory) of (3RS,4RS)-4-(4-chloro-phenyl)-3-(naphthalen-2-ylmethoxy)-piperidine, MS: 210 (M-C11H9)+, which was converted into the hydrochloride of m.p. 159-161° C. (dec.) with a solution of hydrogen chloride in methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051712
Source datasetuspto-grants-2000_04
ORD IDord-96c200bcbd5647f0b430a7de19a86b38
Source noteuspto-grants-2000_04