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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180714Generated: November 2, 2026

Acetonitrile → HCID 10243436, compound

https://huagongshe.com/reaction/1180714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
ReactantN-(4-Chlorophenyl)-2,2,2-trifluoroacetamideHCID 9830—
ReactantDiphenyl chlorophosphateHCID 75654—
SolventEthyl AcetateHCID 8857—
ProductHCID 10243436HCID 1024343678.6%

Reaction Conditions

Temperature82 °C

Reaction Steps

Four grams (17.9 mmol) of 2,2,2-trifluoro-N-(4-chlorophenyl)acetamide, 9.61 g (35.8 mmol) of diphenyl chlorophosphate, 3.62 g (35.8 mmol) of triethylamine, and 20 ml of acetonitrile were introduced into a 50 ml flask and reacted for 16 hours while being refluxed (82° C.). After the reaction, the reaction solution was cooled to room temperature, 16 ml of ethyl acetate was added thereto, and the precipitate was then filtered off. The filtrate was subjected to solvent removal by evaporation, and the crude product thus obtained was purified by column chromatography (silica gel, ethyl acetate:hexane=3:7), resulting in 3.40 g of N-(4-chlorophenyl)-2,2,2-trifluoroacetimidoyl chloride as a yellow liquid (yield: 78.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282609B2
Source datasetuspto-grants-2007_10
ORD IDord-37234f631a154a48bcd61bd4047f8e70
Source noteuspto-grants-2007_10