Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552627Generated: November 2, 2026

Acetyl chloride → HCID 86654453, compound

https://huagongshe.com/reaction/552627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86654452HCID 86654452—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductHCID 86654453HCID 8665445334%

Reaction Steps

In a suspension of 0.10 g of 55% oily sodium hydride suspended in 15 mL of N,N-dimethylformamide, a solution of 0.30 g of N-(6-chloro-2-pyridyl)-4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydro-isoxazole-3-yl]-2-methyl benzoic acid amide in 5 mL of N,N-dimethylformamide was added under cooling with ice and with stirring, and stirred at the same temperature for 10 minutes. After ceasing the generation of hydrogen gas, 0.30 g of acetyl chloride was added, ice bath was removed and continued to stir further for 5 minutes. After the completion of the reaction, the reaction mixture was poured in 20 mL of ice water, extracted with ethyl acetate (50 mL×1), the organic phase was dehydrated with and dried over saturated sodium chloride aqueous solution and then anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography that was eluated with ethyl acetate-hexane (1:2) to obtain 0.11 g of the aimed product as colorless resinous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951828B1
Source datasetuspto-grants-2011_05
ORD IDord-21163f05057f4075832a68aeac2b9383
Source noteuspto-grants-2011_05