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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712104Generated: November 2, 2026

HCID 54103280, compound → HCID 59205190, compound

https://huagongshe.com/reaction/1712104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54103280HCID 54103280—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59205190HCID 59205190—

Reaction Steps

To a solution of 4-benzoyl-pyridine-3-carbaldehyde (114 mg, 0.54 mmol) in THF (3 mL) at −78° C. was added 3.0 M methylmagnesium bromide in THF (0.27 mL) and the reaction mixture was 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 chromatography of silica gel with 5% methanol in dichloromethane to yield [3-(1-hydroxy-ethyl)-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-ebd27aa0864242e7a8f9bfc957f86353
Source noteuspto-grants-2010_09