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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046098Generated: October 31, 2026

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

https://huagongshe.com/reaction/1046098

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Chloropyrimidin-5-yl)ethan-1-oneHCID 13715742—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Chloropyrimidin-5-yl)propan-2-olHCID 1371574751.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-(2-chloropyrimidin-5-yl)ethanone (268 mg, 1.7 mmol) in THF (20 mL) was added MeMgBr (2.68 mL, 8.04 mmol) at −78° C. under nitrogen. The 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 (PE:EA 3:1) to give 2-(2-chloropyrimidin-5-yl)propan-2-ol (150 mg, yield 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569292B2
Source datasetuspto-grants-2013_10
ORD IDord-1e03a37a646048bb874be26cc8541abf
Source noteuspto-grants-2013_10