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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52173Generated: October 29, 2026

Thiophene → 2-[(4-Fluorophenyl)methyl]thiophene

https://huagongshe.com/reaction/52173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantHexaneHCID 8058—
Reactant4-Fluorobenzyl bromideHCID 68021—
ReactantButyllithiumHCID 178418339—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-[(4-Fluorophenyl)methyl]thiopheneHCID 1058390581%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of thiophene (12.6 g, 0.15 mol) in a mixture of anhydrous ether (230 mL) and anhydrous THF (70 mL) was treated dropwise at 0° C. with a 2.5M solution of n-butyllithium in hexane (54.0 mL, 0.134 mol). The mixture was stirred at 0° C. for 1.5 hours and then transferred by cannula into a -78° C. solution of 4-fluorobenzyl bromide (23.6 g, 0.125 mol) containing tetrakis(triphenylphosphine) palladium(0) (1.25 g) in anhydrous THF (200 mL). The reaction mixture was stirred at ambient temperature under nitrogen overnight and then quenched with saturated NH4Cl solution (100 mL) and partitioned between ether and additional NH4Cl solution. The ether layer was dried over MgSO4, concentrated in vacuo and the residue subjected to vacuum distillation to give 19.4 g (81% ) of 2-(4-fluorophenylmethyl)thiophene. b.p. 74°-83° C. at 0.6-0.7 mm of Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616596
Source datasetuspto-grants-1997_04
ORD IDord-c7035b63f308406b8daa8da500a0e393
Source noteuspto-grants-1997_04