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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15651Generated: October 27, 2026

Citric Acid → [4-Hydroxy-3'-(hydroxymethyl)-6-methylbiphenyl-2-yl]methyl acetate

https://huagongshe.com/reaction/15651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant(4-Acetoxy-3'-formyl-6-methylbiphenyl-2-yl)methyl acetateHCID 59342569—
SolventMethanolHCID 887—
Product[4-Hydroxy-3'-(hydroxymethyl)-6-methylbiphenyl-2-yl]methyl acetateHCID 5934261171.4%

Reaction Steps

To a solution of (4-acetoxy-3′-formyl-6-methylbiphenyl-2-yl)methyl acetate (1.63 g, 4.99 mmol) in a mixed solvent of tetrahydrofuran (10 mL) and methanol (5 mL) was added sodium borohydride (90%, 0.210 g, 5.00 mmol) under ice-cooling, and the mixture was stirred at the same temperature for 3 hr under nitrogen atmosphere. Aqueous citric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=20:80-80:20) to give the title compound (1.02 g, yield 71%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732626B2
Source datasetuspto-grants-2010_06
ORD IDord-52669a6c8066414c842d8e726fb9b71a
Source noteuspto-grants-2010_06