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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712072Generated: October 25, 2026

4-Bromopyridine-3-carbaldehyde → 1-(4-Bromo-pyridin-3-yl)-2-methyl-propan-1-ol

https://huagongshe.com/reaction/1712072

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromopyridine-3-carbaldehydeHCID 11116740—
ReactantHCID 178418365HCID 178418365—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromo-pyridin-3-yl)-2-methyl-propan-1-olHCID 59205192—

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 1.0 M isopropyl-magnesium bromide solution in THF (3.23 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 1-(4-bromo-pyridin-3-yl)-2-methyl-propan-1-ol as slight yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790895B2
Source datasetuspto-grants-2010_09
ORD IDord-db9281c220384cdb9385a95dea3da23b
Source noteuspto-grants-2010_09