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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827887Generated: October 25, 2026

Triethylamine → Ethyl 5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazole-3-carboxylate

https://huagongshe.com/reaction/1827887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethenyl-4-(trifluoromethyl)benzeneHCID 2782798—
ReactantEthyl 2-chloro-2-(hydroxyamino)acetateHCID 22064134—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazole-3-carboxylateHCID 22064077—

Reaction Steps

To a mixture of 1-(trifluoromethyl)-4-vinylbenzene (2.0 g, 11.27 mmol), a compound of formula (20) and ethyl 2-chloro-2-(hydroxyamino)acetate (2.11 g, 13.52 mmol), a compound of formula (21), in anhydrous THF was added a solution of triethylamine (3.0 ml) in tetrahydrofuran was added dropwise at room temperature. The mixture was stirred overnight under N2. The white precipitate thus formed was filtered off, and washed twice with tetrahydrofuran (10 ml). The solvent was removed from the filtrate under reduced pressure, and the residue partitioned between water/ethyl acetate (20 ml:20 ml v/v), extracting three times with 20 ml of ethyl acetate. The combined organic layers were washed with aqueous ammonium chloride, and dried over MgSO4, to provide ethyl 5-[4-(trifluoromethyl)phenyl]-4,5-dihydroisoxazole-3-carboxylate, a compound of formula (22).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056924B2
Source datasetuspto-grants-2006_06
ORD IDord-4fa9d205e4504e8882f4f8c13f3d8b56
Source noteuspto-grants-2006_06