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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354972Generated: October 31, 2026

1-Bromo-3-(4-methoxy-but-1-enyl)-benzene → 1-Bromo-3-(4-methoxybutyl)benzene

https://huagongshe.com/reaction/2354972

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-(4-methoxy-but-1-enyl)-benzeneHCID 67542386—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-3-(4-methoxybutyl)benzeneHCID 57435896—

Reaction Steps

A suspension of the title B compound, 1-bromo-3-(4-methoxy-but-1-enyl)-benzene (1.8 g, 7.46 mmol) and Pd/c 5% (0.36 g) in THF (20 mL) is shaked under an hydrogen atmosphere. After completion of the reaction, the mixture is filtered through a pad of celite, the solvent is evaporated under reduced pressure and the residue purified by flash chromatography on silica gel (hexane/EtOAc 98/2) to give the title compound as a yellow oil: MS 260.1, 261.9 [M+18]. Rt (HPLC, Nucleosil C18, 10:90-100:0 CH3CN/H2O+0.1% TFA within 5 min, then 100% CH3CN+0.1% TFA): 6.45 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754727B2
Source datasetuspto-grants-2010_07
ORD IDord-fafc85bb3d8b4a91948504fa903922d5
Source noteuspto-grants-2010_07