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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180706Generated: November 3, 2026

Acetonitrile → HCID 11775698, compound

https://huagongshe.com/reaction/1180706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
ReactantDiphenyl chlorophosphateHCID 75654—
ReactantAcetamide, 2,2,2-trifluoro-N-(4-methylphenyl)-HCID 136175—
SolventEthyl AcetateHCID 8857—
ProductHCID 11775698HCID 1177569888.6%

Reaction Conditions

Temperature82 °C

Reaction Steps

Seven grams (34.5 mmol) of 2,2,2-trifluoro-N-(4-methylphenyl)acetamide, 18.49 g (68.9 mmol) of diphenyl chlorophosphate, 6.97 g (68.9 mmol) of triethylamine, and 35 ml of acetonitrile were introduced into a 100 ml flask and reacted for 18 hours while being refluxed (82° C.). After the reaction, the reaction solution was cooled to room temperature, 25 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 6.77 g of N-(4-methylphenyl)-2,2,2-trifluoroacetimidoyl chloride as a yellow liquid (yield: 88.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282609B2
Source datasetuspto-grants-2007_10
ORD IDord-0adf829e6bd2401dabb239807a649bcb
Source noteuspto-grants-2007_10