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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975747Generated: November 1, 2026

Furan → 2-(4-Fluorophenylmethyl)furan

https://huagongshe.com/reaction/1975747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuranHCID 8029—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Fluorobenzyl bromideHCID 68021—
ReactantButyllithiumHCID 178418339—
CatalystHCID 178418397HCID 178418397—
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 (0) (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 the title compound 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 numberUS05288751
Source datasetuspto-grants-1994_02
ORD IDord-8c2ad678073547b5970d83ec19c1d054
Source noteuspto-grants-1994_02