돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58571생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/58571

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Sodium CarbonateHCID 10340—
반응물(2,5-Difluorophenyl)boronic acidHCID 2734335—
반응물Ethyl 5-(bromomethyl)-1,2-oxazole-3-carboxylateHCID 13124955—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
생성물Ethyl 5-(2,5-difluorobenzyl)isoxazole-3-carboxylateHCID 6683191559%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434722B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-56c06f3f570d491c85ebf3b41cfd0baa
출처 메모uspto-grants-2016_09