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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293007Generated: October 30, 2026

4-Hydroxybiphenyl → HCID 22878842, compound

https://huagongshe.com/reaction/2293007

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybiphenylHCID 7103—
Reactantalpha-D-Galactopyranosyl bromide, tetraacetateHCID 102932—
SolventAcetoneHCID 180—
SolventPotassium HydroxideHCID 14797—
ProductHCID 22878842HCID 22878842—

Reaction Steps

To a solution of p-phenylphenol (250 mg, 1.46 mmol) in acetone, 1 mL of 10N KOH was added followed by acetobromogalactose (1.8 g, 4.37 mmol). The reaction mixture was stirred overnight at room temperature. TLC analysis showed no starting material left. 10N KOH (1 mL) was added to complete deacetylation and the solution was again stirred overnight. After evaporation of acetone, the crude material was taken up in ethyl acetate and washed with 5×150 mL of water. Ethyl acetate was dried with MgSO4 and concentrated under reduced pressure to obtain a white solid which was further purified by column chromatography using 30% methanol/ethyl acetate; 1H NMR (CD3OD) δ3.56-3.91 (m, 6H), 4.89 (m, 1H), 7.15-7.57 (m,9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686258
Source datasetuspto-grants-1997_11
ORD IDord-e76b77cfce624f2abd8e9d78dd1e98a8
Source noteuspto-grants-1997_11