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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551306Generated: October 29, 2026

Triethylamine → Methyl 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]benzoate

https://huagongshe.com/reaction/551306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
ReactantMethyl 4-(hydroxyiminomethyl)benzoateHCID 6804457—
Reactant1,3-Dichloro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzeneHCID 23159823—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]benzoateHCID 6678550768.7%

Reaction Conditions

Temperature40 °C

Reaction Steps

In a solution of 2.70 g of methyl 4-(hydroxyiminomethyl)benzoate in 15 mL of N,N-dimethylformamide, 2.04 g of N-chlorosuccinimide was added, and stirred at 40° C. for 40 minutes. Then, the reaction mixture was cooled to 0° C., 3.40 g of 3,5-dichloro-1-(1-trifluoromethylethenyl)benzene and 1.72 g of triethylamine were added, and continued to stir at room temperature further for 18 hours. After the completion of the reaction, the reaction mixture was poured into 100 mL of ice water, extracted with ethyl acetate (50 mL×2), the organic phase was washed with water and then dehydrated with and dried over saturated sodium chloride aqueous solution and anhydrous sodium sulfate in that order, and the solvent was distilled off under reduced pressure. The residual solid was purified with medium pressure preparative liquid chromatography (medium pressure collection apparatus: YFLC-Wprep manufactured by Yamazen Corporation) that was eluted with ethyl acetate-hexane (gradient of 1:1 to 1:3) to obtain 4.05 g of the aimed products as white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947715B2
Source datasetuspto-grants-2011_05
ORD IDord-6dc15c6e4a274f9cbe5b6cffed883b2e
Source noteuspto-grants-2011_05