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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989600Generated: October 25, 2026

Hydrochloric Acid → 2-(4,6-Dimethoxypyrimidine-2-yl)-2-(2-nitrophenyl)acetonitrile

https://huagongshe.com/reaction/989600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-NitrophenylacetonitrileHCID 11888—
ReactantSodium hydrideHCID 24758—
Reactant4,6-Dimethoxy-2-(methylsulfonyl)pyrimidineHCID 838363—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(4,6-Dimethoxypyrimidine-2-yl)-2-(2-nitrophenyl)acetonitrileHCID 1841799079.2%

Reaction Steps

50 g (0.31 M) of 2-(2-nitrophenyl)acetonitrile was dissolved in 500 ml of dimethylformamide. Thereto was added 24.7 g (0.62 M) of 60% sodium hydride. The mixture was stirred at room temperature for 2 hours. Then, 68 g (0.31 M) of 4,6-dimethoxy-2-methanesulfonylpyrimidine was added. The mixture was stirred at 80° C. for 1 hour to give rise to a reaction. The reaction mixture was poured into water, followed by neutralization with dilute hydrochloric acid. The mixture was subjected to extraction with ethyl acetate. The extract was washed with water, dried and subjected to vacuum distillation to remove the solvent. The residue was recrystallized from ethanol to obtain 73.3 g (yield: 79%) of 2-(4,6-dimethoxypyrimidine-2-yl)-2-(2-nitrophenyl)acetonitrile as a white powder (melting point: 88 to 89° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458748B1
Source datasetuspto-grants-2002_10
ORD IDord-dd022a877f0f4698bbe28d430fdf74a2
Source noteuspto-grants-2002_10