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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910356Generated: October 28, 2026

Sodium Hydroxide → 4-[5-(3,5-Dichlorophenyl)-5-trifiuoromethyl-4,5-dihydroisoxazol-3-yl]-2-methoxy benzoic acid

https://huagongshe.com/reaction/910356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-[5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methoxybenzoic acid ethyl esterHCID 66785501—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-[5-(3,5-Dichlorophenyl)-5-trifiuoromethyl-4,5-dihydroisoxazol-3-yl]-2-methoxy benzoic acidHCID 6678497499.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

In a solution of 1.07 g of 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]-2-methoxy benzoic acid ethyl ester in 30 ml of ethanol, a solution of 1.0 g of sodium hydroxide in 30 ml of water was added, stirred at 85° C. for 1 hour. After the completion of the reaction, the solvent was distilled off under reduced pressure. The residue was adjusted to pH 2 to 3 with concentrated hydrochloric acid, and extracted with ethyl acetate (30 ml×2). The organic phase was dehydrated with saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to obtain 1.0 g of the aimed product as pale yellow resinous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022089B2
Source datasetuspto-grants-2011_09
ORD IDord-74d85c97efb24871b37a2a12bf93f56f
Source noteuspto-grants-2011_09