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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873431Generated: November 2, 2026

2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-vinylselenophene → 2-Ethyl-5-(4'-ethyl-3-fluorobiphenyl-4-yl)selenophene

https://huagongshe.com/reaction/1873431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-vinylselenopheneHCID 59456356—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-Ethyl-5-(4'-ethyl-3-fluorobiphenyl-4-yl)selenopheneHCID 59456259—

Reaction Steps

3.10 g (8.73 mmol) of 2-(4′-ethyl-3-fluorobiphenyl-4-yl)-5-vinylselenophene are hydrogenated in 30 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-Ethyl-5-(4′-ethyl-3-fluorobiphenyl-4-yl)selenophene is obtained as a colourless solid (m.p. 110° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304036B2
Source datasetuspto-grants-2012_11
ORD IDord-28c3632568d944baa9868fafec175fbe
Source noteuspto-grants-2012_11