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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 338086생성일: 2026년 10월 25일

Ethanol → 5-Allyl-6a-(2-fluorophenyl)-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]isoxazole

https://huagongshe.com/reaction/338086

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물PyridineHCID 1049—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물2-Bromo-2'-fluoroacetophenoneHCID 2737449—
생성물5-Allyl-6a-(2-fluorophenyl)-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]isoxazoleHCID 8669789858%

반응 단계

To a solution of 2-bromo-1-(2-fluorophenyl)ethanone (10.0 g, 46.1 mmol) in ethanol (460.8 mL) is added drop wise diallyamine (9.4 g, 96.8 mmol) in ethanol (460.8 mL). The reaction is stirred for 2 hr. Pyridine is then added to the reaction (11.2 mL, 138.2 mmol) followed by the addition of hydroxylamine hydrochloride (4.8 g, 69.1 mmol). The reaction is refluxed for 4 hr and then concentrated to dryness. The residue is dissolved in toluene (230.4 mL) and is refluxed for 8 hr. The mixture is cooled to room temperature and extracted with saturated sodium bicarbonate solution. The aqueous phase is then extracted with DCM. The organic phase is concentrated and the mixture purified by silica gel chromatography eluting with hexane to 1:1 hexane/ethyl acetate to give the title compound (6.6 g, 58%). ES/MS (m/e): 248 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889856B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-1ea8249382284ce0b897ac968550fdba
출처 메모uspto-grants-2014_11