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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738683Generated: November 1, 2026

5-Bromo-2-[2-(4-methoxyphenyl)vinyl]benzofuran → 5-Bromo-2-[2-(4-methoxyphenyl)ethyl]benzofuran

https://huagongshe.com/reaction/1738683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-[2-(4-methoxyphenyl)vinyl]benzofuranHCID 53780930—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-[2-(4-methoxyphenyl)ethyl]benzofuranHCID 2184431075.4%

Reaction Steps

128 g of 5-bromo-2-[2-(4-methoxyphenyl)vinyl]benzofuran as a mixture of two stereoisomers was dissolved in a solvent mixture of 1.3 l of tetrahydrofuran and 0.7 l of ethanol. The resulting solution was mixed with 3.0 g of platinum dioxide and subjected to 4 hours of catalytic hydrogenation under normal pressure. Thereafter, the catalyst was removed by filtration, the resulting filtrate was concentrated, and crystals thus precipitated were collected by filtration and washed with ethanol. In this way, 97.08 g of 5-bromo-2-[2-(4-methoxyphenyl)ethyl]benzofuran was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962695
Source datasetuspto-grants-1999_10
ORD IDord-61baa9083f88402198f2e4ed6d67c93d
Source noteuspto-grants-1999_10