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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587586Generated: October 31, 2026

Tetrahydrofuran → 4-Hydroxy-4'-(1-hydroxyethyl)biphenyl

https://huagongshe.com/reaction/1587586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Methylcarbonyloxy-4'-hydroxybiphenylHCID 14438409—
SolventMethanolHCID 887—
Product4-Hydroxy-4'-(1-hydroxyethyl)biphenylHCID 1393080092.9%

Reaction Steps

A solution containing 4-acetoxy-4'-hydroxy-1,1'-biphenyl from part A (5.0 g, 23.6 mmol) in methanol (500 mL) and tetrahydrofuran (30 mL) is treated with sodium borohydride (0.9 g, 23.8 mmol) in portions over 30 minutes at room temperature. After 2 hours, the reaction mixture is concentrated under reduced pressure, diluted with water (400 mL), acidified with 2N HCl and extracted with ethyl acetate. The organic layer is washed with water and brine, dried over MgSO4 and concentrated to a solid residue. Crystallization of the solid from ethyl acetate gives 4.7 g (92.9%) of the title compound, m.p. 159°-160° C.; MS (EI m/z): 214 (M)+ and 199 (b.p. M--CH3)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05218124
Source datasetuspto-grants-1993_06
ORD IDord-300177ea7ab14f11b5bd5c26b0c9fdb8
Source noteuspto-grants-1993_06