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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1827887Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1827887

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-Ethenyl-4-(trifluoromethyl)benzeneHCID 2782798—
EduktEthyl 2-chloro-2-(hydroxyamino)acetateHCID 22064134—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazole-3-carboxylateHCID 22064077—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07056924B2
Quelldatensatzuspto-grants-2006_06
ORD IDord-4fa9d205e4504e8882f4f8c13f3d8b56
Quellennotizuspto-grants-2006_06