Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474358Generated: October 29, 2026

Hydroxyamine hydrochloride → Ethyl 5-(2-(trifluoromethyl)phenyl)isoxazole-4-carboxylate

https://huagongshe.com/reaction/474358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant3-Dimethylamino-2-(2-trifluoromethyl-benzoyl)-acrylic acid ethyl esterHCID 54042795—
SolventMethanolHCID 887—
ProductEthyl 5-(2-(trifluoromethyl)phenyl)isoxazole-4-carboxylateHCID 2029749851.2%

Reaction Steps

A mixture of 3-dimethylamino-2-(2-trifluoromethyl-benzoyl)-acrylic acid ethyl ester (3.10 g, 9.80 mmol, 1.0 equiv) and hydroxylamine hydrochloride (683 mg, 9.80 mmol, 1.0 equiv) in methanol (25 mL) was heated to reflux for 90 minutes. After cooling, the mixture was partitioned between water and ethyl acetate and separated. The aqueous layer was extracted with ethyl acetate. The combined organic extracts was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. Purification by flash column chromatography on silica gel (gradient: 0 to 30% ethyl acetate in cyclohexane) gave 1.43 g (51%) of 5-(2-trifluoromethyl-phenyl)-isoxazole-4-carboxylic acid ethyl ester. 1H NMR (300 MHz, CDCl3) δ: 8.38 (s, 1H), 7.69 (d, 1H), 7.61-7.47 (m, 2H), 7.27 (d, 1H), 3.93 (br, 2H), 0.87 (br, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637526B2
Source datasetuspto-grants-2014_01
ORD IDord-6529b7cc8f27482e819a06fca576e731
Source noteuspto-grants-2014_01