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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407074Generated: October 30, 2026

2-Cyanopyrimidine → 1-(Pyrimidin-2-yl)ethan-1-one

https://huagongshe.com/reaction/2407074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-CyanopyrimidineHCID 2757979—
ReactantChloroform methanolHCID 21584188—
ReactantHCID 178418573HCID 178418573—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(Pyrimidin-2-yl)ethan-1-oneHCID 1160790948%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-cyano-pyrimidine (10.0 g, 95.2 mmol) in THF (100 mL) was cooled to −5° C. and treated with a 3 M solution of methyl magnesium bromide in THF (38.0 mL, 98.4 mmol). The reaction was stirred at 0° C. for two hours until completion was observed by TLC (chloroform/methanol, 9:1). The reaction mixture was poured in water; the pH was adjusted to 5-6 and the aqueous layer was extracted with ethyl acetate (3×150 mL). The combined organic layers were concentrated under reduced pressure and the crude compound was purified by column chromatography, eluting with chloroform to afford the target compound (6.5 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809525B2
Source datasetuspto-grants-2014_08
ORD IDord-0688f7242006440f84ee49ea5620c741
Source noteuspto-grants-2014_08