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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180341Generated: October 31, 2026

Pyridine → 4'-Hydroxy-3-methyl[1,1'-biphenyl]-4-carbaldehyde oxime

https://huagongshe.com/reaction/1180341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant4'-Hydroxy-3-methyl[1,1'-biphenyl]-4-carbaldehydeHCID 58978535—
SolventMethanolHCID 887—
Product4'-Hydroxy-3-methyl[1,1'-biphenyl]-4-carbaldehyde oximeHCID 13633859553.3%

Reaction Steps

A mixture of 4′-hydroxy-3-methyl[1,1′-biphenyl]-4-carbaldehyde (310 mg, 1.46 mmol), hydroxylamine hydrochloride (203 mg, 2.92 mmol) and pyridine (236 ul, 2.92 mmol) in 15 mL absolute methanol was refluxed for 2.5 h. The solvent was removed under reduced pressure and the mixture was dissolved in ethyl acetate and water, extracted with ethyl acetate (×3), washed with brine, dried over sodium sulfate, and filtered. Evaporation of the solvent and purification by recrystallization (ethyl acetate, acetone and hexane) gave 177 mg (53%) of the title compound as a yellowish solid: mp 195-197° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279600B2
Source datasetuspto-grants-2007_10
ORD IDord-21fd4b15355241d69a6a548fdafd7108
Source noteuspto-grants-2007_10