Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709607Generated: October 29, 2026

Hydrochloric Acid → Cyclopropyl(6-methoxypyrimidin-4-yl)methanone

https://huagongshe.com/reaction/709607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Methoxypyrimidine-4-carbonitrileHCID 59238022—
ReactantHCID 178418630HCID 178418630—
SolventTetrahydrofuranHCID 8028—
ProductCyclopropyl(6-methoxypyrimidin-4-yl)methanoneHCID 91618935—

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere, to a solution of 6-methoxypyrimidine-4-carbonitrile (6.00 g) in THF (120 mL) was added dropwise a 0.52 M solution of cyclopropylmagnesium bromide in THF (215 mL) at 0° C., and the mixture was stirred at 0° C. for 1 hr. 6N Hydrochloric acid (60 mL) was added to the reaction mixture at 0° C., and the mixture was stirred at room temperature for 15 min. The reaction mixture was neutralized with sodium hydrogen carbonate (35.0 g), and extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give a crude product of the title compound as a brown oil. This compound was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-a2391facef1a4361924c5d803b42405e
Source noteuspto-grants-2015_11