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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725660Generated: October 30, 2026

4-Methoxy-3-(4-methoxy-2-butenyl)-bromobenzene → 4-Bromo-1-methoxy-2-(4-methoxybutyl)benzene

https://huagongshe.com/reaction/725660

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-3-(4-methoxy-2-butenyl)-bromobenzeneHCID 54142774—
CatalystPlatinumHCID 23939—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-1-methoxy-2-(4-methoxybutyl)benzeneHCID 21458627—

Reaction Steps

A solution of 50 g of 4-methoxy-3-(4-methoxy-2-butenyl)-bromobenzene in 700 ml of tetrahydrofuran is hydrogenated for 2 hours under normal pressure and at room temperature in the presence of 2.5 g of 5% Pt/C. The reaction mixture is filtered. The filtrate is concentrated by evaporation. The evaporation residue obtained from the filtrate is purified by PC (1.6 kg of silica gel, hexane/ethyl acetate=20:1). Distillation under a high vacuum yields the title compound: Rf (hexane/ethyl acetate=10:1)=0.38; HPLC Rt =19.92 minutes; FAB-MS (M+H)+ =273.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705658
Source datasetuspto-grants-1998_01
ORD IDord-86264525305646d6ace8dd7ea984aeb3
Source noteuspto-grants-1998_01