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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52164Generated: October 29, 2026

Furan → 2-(4-Fluorophenylmethyl)furan

https://huagongshe.com/reaction/52164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuranHCID 8029—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Fluorobenzyl bromideHCID 68021—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Fluorophenylmethyl)furanHCID 1996329181.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of furan (13.6 g, 0.20 mol) in a mixture of anhydrous ether (230 mL) and anhydrous THF (70 mL) under nitrogen was added 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 to a stirred -78° C. solution of 4-fluorobenzyl bromide (23.6 g, 0.125 mol) and tetrakis-(triphenylphosphine)palladium (O) (1.25 g, 0.001 mol) in anhydrous THF (200 mL). The transfer was made under nitrogen over a period of 30-40 minutes. The reaction mixture was stirred at ambient temperature overnight, saturated aqueous solution of ammonium chloride was added and the mixture extracted with ether. The ether layer was dried (MgSO4), concentrated in vacuo and the residue distilled at reduced pressure to give 2-(4-fluorophenylmethyl)furan as a colorless oil (17.89 g, 81% ). b.p. 57°-62° C. at 0.5-0.7 mm-Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616596
Source datasetuspto-grants-1997_04
ORD IDord-e27ba103370d43dd91c69944a80b85e4
Source noteuspto-grants-1997_04