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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552660Generated: November 1, 2026

Acetyl chloride → HCID 67165879, compound

https://huagongshe.com/reaction/552660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 67163670HCID 67163670—
SolventDichloromethaneHCID 6344—
ProductHCID 67165879HCID 6716587995.4%

Reaction Steps

In a solution of 0.20 g of 2-amino-4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]benzoic acid amide and 0.12 g of triethylamine in 5 mL of dichloromethane, 0.05 g of acetyl chloride was added under cooling with ice and with stirring, and stirred at room temperature for 40 minutes. After the completion of the reaction, 10 mL of ethyl acetate was added in the reaction mixture, and washed with 10 mL of water, 10 mL of saturated sodium hydrogen carbonate aqueous solution, and then 10 mL of saturated ammonium chloride aqueous solution in that order. The organic phase was dehydrated with and dried over saturated sodium chloride aqueous solution and then anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 0.21 g of the crude aimed product as yellow crystal. The resulting product was used as such without purification for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951828B1
Source datasetuspto-grants-2011_05
ORD IDord-732bc334a5d94c9baa5f0aa662a28a39
Source noteuspto-grants-2011_05