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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712103Generated: November 1, 2026

HCID 54103280, compound → HCID 59205203, compound

https://huagongshe.com/reaction/1712103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54103280HCID 54103280—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59205203HCID 59205203—

Reaction Steps

To a solution of 4-benzoyl-pyridine-3-carbaldehyde (97 mg, ol) in THF (5 mL) at −78° C. was added 1.0M phenylmagnesium bromide in THF (0.46 mL) and the reaction mixture stirred for 15 min. The reaction mixture was then quenched with aqueous ammonium chloride and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, concentrated, and the residue purified by preparation TLC of silica gel with 10% methanol in dichloromethane to yield [3-(hydroxy-phenyl-methyl)-pyridin-4-yl]-phenyl-methanone as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790895B2
Source datasetuspto-grants-2010_09
ORD IDord-2e0e265157eb4710b18b755ed8c0aa80
Source noteuspto-grants-2010_09