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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509165Generated: October 30, 2026

Furfural → HCID 67109386, compound

https://huagongshe.com/reaction/509165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
ReactantHexaneHCID 8058—
Reactant5-Fluoro-2-iodo-1,3-dimethylbenzeneHCID 67109268—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67109386HCID 6710938661.9%

Reaction Conditions

Temperature-75 °C

Reaction Steps

To a solution of 5-fluoro-2-iodo-1,3-xylene (11 g, 44 mmol) in tetrahydrofuran (110 ml) is added 1.6 molar solution of n-butyl lithium in hexane (33 ml, 52 mmol) under nitrogen atmosphere at −75° C. The resulting solution is stirred at −75° C. for 60 minutes and to this mixture, a solution of furfural (6.3 g, 65.6 mmol) in THF (20 ml) is added over 20 minutes. The resulting solution is stirred at −75° C. for 2 hours. The cooling bath is removed and the mixture is allowed to reach room temperature, and then stirred for 5 hours. The reaction mixture is quenched with ice cold water (1000 ml) and extracted with ethyl acetate (3×250 ml), dried over anhydrous sodium sulphate, filtered and the filtrate is concentrated in vacuo to give a residue which is purified by flash chromatography (hexane/ethyl acetate) to afford (4-Fluoro-2,6-dimethylphenyl)furan-2-ylmethanol (6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096560B2
Source datasetuspto-grants-2015_08
ORD IDord-5def3c44b574403bb7c2c9befb3c2415
Source noteuspto-grants-2015_08