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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046103Generated: October 26, 2026

1-(5-Bromopyrimidin-2-yl)ethan-1-one → 2-(5-Bromopyrimidin-2-yl)propan-2-ol

https://huagongshe.com/reaction/1046103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Bromopyrimidin-2-yl)ethan-1-oneHCID 53488064—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product2-(5-Bromopyrimidin-2-yl)propan-2-olHCID 5848528646.77%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-(5-bromopyrimidin-2-yl)ethanone (99 mg, 0.50 mmol) in THF (10 mL) was added MeMgBr (1.65 mL, 4.95 mmol) at −78° C. under nitrogen. The formed solution was stirred at −78° C. for 20 min, quenched with satd aq NH4Cl, and extracted with EtOAc. The combined organic layer was dried over anhydrous Na2SO4 and concentrated to give an oil, which was purified by prep TLC (3:1 PE/EtOAc) to give 2-(5-bromopyrimidin-2-yl)propan-2-ol (50 mg, yield: 46.77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569292B2
Source datasetuspto-grants-2013_10
ORD IDord-6601085bd313461aa1c2e3612db19e05
Source noteuspto-grants-2013_10