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HRID 58944Erstellt: 24. Oktober 2026

Chlorosuccinimide → 5-((2,6-Difluorobenzyloxy)methyl)-3-(2-fluorophenyl)-5-methyl-4,5-dihydroisoxazole

https://huagongshe.com/de/reaction/58944

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorosuccinimideHCID 31398—
EduktSodium BicarbonateHCID 516892—
EduktBenzaldehyde, 2-fluoro-, oximeHCID 587025—
Edukt1,3-Difluoro-2-((2-methylallyloxy)methyl)benzeneHCID 11264071—
KatalysatorTetrabutylammonium IodideHCID 67553—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-((2,6-Difluorobenzyloxy)methyl)-3-(2-fluorophenyl)-5-methyl-4,5-dihydroisoxazoleHCID 8949186779,9%

Reaktionsschritte

200 mg of 2-fluorobenzaldehyde oxime was dissolved in 4 mL of 1,2-dichloroethane, and then, 230 mg of N-chlorosuccinimide and 0.4 mL of dimethylformamide were slowly added thereto at a temperature of 0° C. The reaction mixture was stirred at room temperature for 1 hour, and then, the reaction state was confirmed by TLC. When the oxime, which was a starting material, disappeared, the reaction mixture was cooled to a temperature 0° C., and then, 182 mg of NaHCO3, 27 mg of tetrabutylammonium iodide, and 342 mg of 1,3-difluoro-2-((2-methylallyloxy)methyl)benzene were sequentially, slowly added thereto. The reaction mixture was stirred at room temperature overnight, and then, diluted with dichloromethane, and then, washed with water, and the obtained organic layer was dried by using magnesium sulfate and concentrated, and the concentrate was separated by silicagel column chromatography to obtain 385 mg of 5-((2,6-difluorobenzyloxy)methyl)-3-(2-fluorophenyl)-5-methyl-4,5-dihydroisoxazole.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09439432B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-bc440beb8dc04a50ba36f8a9ea5a7946
Quellennotizuspto-grants-2016_09