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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53969Generated: October 29, 2026

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

https://huagongshe.com/reaction/53969

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 undernormal 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 numberUS05620991
Source datasetuspto-grants-1997_04
ORD IDord-9ec95cac91ae4b4c8aea3a09fdf7d211
Source noteuspto-grants-1997_04