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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393148Generated: October 30, 2026

Acetonitrile → HCID 12151353, compound

https://huagongshe.com/reaction/393148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12151356HCID 12151356—
SolventWaterHCID 962—
ProductHCID 12151353HCID 1215135370.3%

Reaction Steps

8.3 g (0.031 mol) of [1-(4-diethoxymethylpyrimidin-5-yl)-2-methylpropyl]methylamine and 6.4 g (46 mmol) of potassium carbonate were added to 100 ml of acetonitrile, and then 5.8 g (0.038 mol) of phenylacetyl chloride was dropwise added at room temperature and reacted for 2 hours. After completion of the reaction, the product was poured into water and extracted with ethyl acetate. The organic layer was washed with an aqueous citric acid solution, water and an aqueous sodium chloride solution in this order, dried and concentrated, and the obtained oily product was purified by silica gel column chromatography (ethyl acetate:n-hexane=1:5 to ethyl acetate), to obtain 8.4 g (yield: 70%) of N-[1-(4-diethoxymethylpyrimidin-5-yl)-2-methylpropyl]-N-methyl-2-phenyl acetamide as colorless viscous liquid (nD2=1.5253)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806230B1
Source datasetuspto-grants-2004_10
ORD IDord-c671939eaf8c42acaa2cb19b5fa7318f
Source noteuspto-grants-2004_10