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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016435Generated: October 27, 2026

Tert-butyl 4-(4-chlorobenzylidene)piperidine-1-carboxylate → Tert-butyl 4-(4-chlorobenzyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1016435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4-chlorobenzylidene)piperidine-1-carboxylateHCID 22893850—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
ProductTert-butyl 4-(4-chlorobenzyl)piperidine-1-carboxylateHCID 2289385199.3%

Reaction Steps

A solution of 2 g of 4-(4-chloro-benzylidene)-piperidine-1-carboxylic acid tert-butyl ester and 0.5 g of 5% platinum on carbon in 10 mL of ethanol was allowed to stir overnight under 1 atm of hydrogen. The catalyst was filtered off and, the solution concentrated to give 2 g of 4-(4-chloro-benzyl)-piperidine-1-carboxylic acid tert-butyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476041B1
Source datasetuspto-grants-2002_11
ORD IDord-4e1c8dc359394203ba0dae17b6a8ba8b
Source noteuspto-grants-2002_11