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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873402Generated: November 2, 2026

2-(4-Ethoxy-2,3-difluorophenyl)-5-but-1-enylselenophene → 2-(4-Ethoxy-2,3-difluorophenyl)-5-butylselenophene

https://huagongshe.com/reaction/1873402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Ethoxy-2,3-difluorophenyl)-5-but-1-enylselenopheneHCID 72290248—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-(4-Ethoxy-2,3-difluorophenyl)-5-butylselenopheneHCID 59456300—

Reaction Steps

2.30 g (6.22 mmol) of 2-(4-ethoxy-2,3-difluorophenyl)-5-but-1-enylselenophene are hydrogenated in 70 ml of ethyl acetate, in the presence of Pd/C (5% of Pd) at atmospheric pressure and RT. The reaction soln. is filtered and concentrated to dryness, and the crude product is purified by recrystallisation from n-heptane. 2-(4-Ethoxy-2,3-difluorophenyl)-5-butylselenophene is obtained as a colourless solid (m.p. 47° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304036B2
Source datasetuspto-grants-2012_11
ORD IDord-256a354663ba448cb85aae320f3dcfb0
Source noteuspto-grants-2012_11