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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242111Generated: November 2, 2026

4-Bromopyridine-3-carbaldehyde → HCID 21600779, compound

https://huagongshe.com/reaction/2242111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromopyridine-3-carbaldehydeHCID 11116740—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21600779HCID 21600779—

Reaction Steps

To a solution of 4-bromo-pyridine-3-carbaldehyde (400 mg, 2.15 mmol) in THF (10 mL) at −78° C. was added dropwise 3.0 M phenylmagnesium bromide solution in THF (1.08 mL). After 15 min, the reaction was quenched with saturated ammonium chloride solution and extracted with ethyl acetate, then purification by flash chromatography eluted with 50% ethyl acetate in hexane to yield (4-bromo-pyridin-3-yl)-phenyl-methanol as slight yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671065B2
Source datasetuspto-grants-2010_03
ORD IDord-366fa280f9d34452855ab4783400c3f8
Source noteuspto-grants-2010_03