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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55614생성일: 2026년 10월 24일

Acetonitrile → 3-(4-(6-Fluorobenzo[d]isoxazol-3-yl)piperidin-1-yl)propan-1-ol

https://huagongshe.com/ko/reaction/55614

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium CarbonateHCID 11430—
반응물3-Bromo-1-propanolHCID 12308—
반응물3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
용매WaterHCID 962—
생성물3-(4-(6-Fluorobenzo[d]isoxazol-3-yl)piperidin-1-yl)propan-1-olHCID 1538496663.9%

반응 단계

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (10.0 g, 45 mmol), K2CO3 (10.0 g), 3-bromo-1-propanol (7.3 g, 46 mmol) and acetonitrile (200 ml) was refluxed for 3 hours. The reaction was poured into H2O and 7.1 g of a beige solid was collected. The filtrate was extracted with dichloromethane, and after concentration an additional 6.7 g of crude solid was harvested. The solids were combined and triturated with refluxing ethyl acetate to afford 8.0 g of 6-fluoro-3-[1-(3-hydroxypropyl)-4-piperidinyl]-1,2-benzisoxazole as an off-white solid. A sample (4.0 g) was recrystallized from ethanol-water (with charcoal treatment) to yield 2.4 g (40%) of the alcohol as a white solid, m.p.=140°-142° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624927
출처 데이터셋uspto-grants-1997_04
ORD IDord-c338c1af5bcf4f199c63b6dd979ff91c
출처 메모uspto-grants-1997_04