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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873433Generated: October 31, 2026

2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-(pent-1-enyl)selenophene → HCID 59456308, compound

https://huagongshe.com/reaction/1873433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4'-Ethyl-3-fluorobiphenyl-4-yl)-5-(pent-1-enyl)selenopheneHCID 72290245—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 59456308HCID 59456308—

Reaction Steps

17.1 g (43.0 mmol) of 2-(4′-ethyl-3-fluorobiphenyl-4-yl)-5-(pent-1-enyl)-selenophene are hydrogenated in 170 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=98:2→95:5). The further purification is carried out by recrystallisation from ethanol and n-heptane. 2-(4′-Ethyl-3-fluorobiphenyl-4-yl)-5-pentylselenophene is obtained as a colourless solid (m.p. 52° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304036B2
Source datasetuspto-grants-2012_11
ORD IDord-b6ceb9fb80a94c048b1c8ceff5c4d35b
Source noteuspto-grants-2012_11