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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858709Generated: October 31, 2026

Dichloromethane → 2-Bromomethylnaphthalene

https://huagongshe.com/reaction/1858709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-BromophenolHCID 7808—
ReactantBenzyl 7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylateHCID 13186888—
SolventEthyl AcetateHCID 8857—
Product2-BromomethylnaphthaleneHCID 70320—
ProductHCID 22126633HCID 22126633—

Reaction Steps

In an analogous manner to that described in Example 71(a)-(b), from benzyl rac-3-aza-7-oxa-bicyclo[4.1.0]heptane-3-carboxylate by reaction with 4-bromophenol there was obtained (3RS,4RS)-1-[4-(4-bromo-phenoxy)-3-hydroxy-piperidin-1-yl]-2-phenyl-ethanone as a colourless solid [Rf : 0.40 (SiO2, methylene chloride:ethyl acetate=2:1)], alkylation of which with 2-bromomethylnaphthalene gave benzyl (3RS,4RS)-4-(4-bromo-phenyl)-3-(naphthalen-2-ylmethoxy)-piperidine-1-carboxylate as a colourless solid; MS: 454, 456 (M-benzyl)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150526
Source datasetuspto-grants-2000_11
ORD IDord-2d9af37e652d4f2086cba82ce10a74ca
Source noteuspto-grants-2000_11