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HRID 58571作成日:2026年10月25日

1,2-Dimethoxyethane → Ethyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylate

https://huagongshe.com/reaction/58571

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethoxyethaneHCID 8071—
反応物Sodium CarbonateHCID 10340—
反応物(2,5-Difluorophenyl)boronic acidHCID 2734335—
反応物Ethyl 5-(bromomethyl)-1,2-oxazole-3-carboxylateHCID 13124955—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物Ethyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylateHCID 6683191559%

反応手順

1,2-Dimethoxyethane (8 mL) and water (2 mL) were added to the mixture of ethyl 5-(bromomethyl)isoxazole-3-carboxylate (1.00 g; 4.27 mmol), 2,5-difluorophenylboronic acid (0.773 g; 4.70 mmol), tetrakis(triphenylphosphine)palladium(0) (0.248 g; 0.640 mmol) and sodium carbonate (0.911 g; 8.55 mmol). The mixture was irradiated in a microwave oven at 130° C. for 20 minutes. After cooling, the reaction mixture was extracted with ethyl acetate and water. The organic layer was concentrated under reduced pressure and the residue was purified by flash chromatography on silica gel (eluent: 5 to 40% of ethyl acetate in heptane) to give 0.67 g (59%) of ethyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylate as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434722B2
出典データセットuspto-grants-2016_09
ORD IDord-56c06f3f570d491c85ebf3b41cfd0baa
出典メモuspto-grants-2016_09