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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877029Generated: November 2, 2026

Hydrochloric Acid → (2-methyl-5-phenylfuran-3-yl)methanol

https://huagongshe.com/reaction/1877029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactantethyl 2-methyl-5-phenyl-3-furoateHCID 10331426—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(2-methyl-5-phenylfuran-3-yl)methanolHCID 2776433100.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethyl 2-methyl-5-phenyl-3-furancarboxylate (5.7 g) in tetrahydrofuran (30 mL) was added dropwise to a suspension of lithium aluminum hydride (1.0 g) in tetrahydrofuran (30 mL) at 0° C. and, after the completion of the dropwise addition, the mixture was stirred at 0° C. for 30 min. The reaction mixture was treated with 1N hydrochloric acid, poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (4.7 g, 100%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-523c8da57d794baca9819a91d1cf22ce
Source noteuspto-grants-2012_11