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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873439Generated: October 30, 2026

2-But-1-enyl-5-(4'-ethyl-2,3-difluorobiphenyl-4-yl)selenophene → 2-Butyl-5-(4'-ethyl-2,3-difluorobiphenyl-4-yl)selenophene

https://huagongshe.com/reaction/1873439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-But-1-enyl-5-(4'-ethyl-2,3-difluorobiphenyl-4-yl)selenopheneHCID 72290262—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-Butyl-5-(4'-ethyl-2,3-difluorobiphenyl-4-yl)selenopheneHCID 59456270—

Reaction Steps

2.40 g (5.72 mmol) of 2-but-1-enyl-5-(4′-ethyl-2,3-difluorobiphenyl-4-yl)-selenophene are hydrogenated in 25 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 column chromatography (SiO2, n-heptane:toluene=9:1). The further purification is carried out by recrystallisation from ethanol and n-heptane. 2-Butyl-5-(4′-ethyl-2,3-difluorobiphenyl-4-yl)selenophene is obtained as a colourless solid (m.p. 73° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304036B2
Source datasetuspto-grants-2012_11
ORD IDord-d4501e35a5b645d881d3747aa8b87b8a
Source noteuspto-grants-2012_11