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HRID 58944作成日:2026年10月25日

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

https://huagongshe.com/reaction/58944

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorosuccinimideHCID 31398—
反応物Sodium BicarbonateHCID 516892—
反応物Benzaldehyde, 2-fluoro-, oximeHCID 587025—
反応物1,3-Difluoro-2-((2-methylallyloxy)methyl)benzeneHCID 11264071—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒1,2-DichloroethaneHCID 11—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物5-((2,6-Difluorobenzyloxy)methyl)-3-(2-fluorophenyl)-5-methyl-4,5-dihydroisoxazoleHCID 8949186779.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09439432B2
出典データセットuspto-grants-2016_09
ORD IDord-bc440beb8dc04a50ba36f8a9ea5a7946
出典メモuspto-grants-2016_09