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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816330Generated: November 3, 2026

tert-Butyl 4-(3-bromophenoxy)piperidine-1-carboxylate → HCID 22492895, compound

https://huagongshe.com/reaction/1816330

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(3-bromophenoxy)piperidine-1-carboxylateHCID 22492957—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
ProductHCID 22492895HCID 22492895—

Reaction Steps

To a solution of tert-butyl 4-(5-bromophenyloxy)-1-piperidinecarboxylate (12.98 g) in methanol (70 ml) was added 28% sodium methoxide methanol solution (37.8 ml) and the mixture was stirred under refluxing for 4 hours. After cooling, the reaction mixture was evaporated in vacuo. The resulting residue was chromatographed on silica gel (400 ml) eluting with a mixture of n-hexane and ethyl acetate (5:1 v/v). The fractions containing the object compound were collected and evaporated under reduced pressure to give tert-butyl 4-(5-methoxypentyloxy)-1-piperidinecarboxylate (16.31 g). This compound was immediately used as the starting compound for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884774B2
Source datasetuspto-grants-2005_04
ORD IDord-1353573013524c07b1d20d0d8bd2c8ae
Source noteuspto-grants-2005_04