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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275744생성일: 2026년 10월 27일

4-Amino-1-butanol → 4-(1,2-Benzisoxazol-3-ylamino)-1-butanol

https://huagongshe.com/reaction/275744

반응식

참여 물질

역할이름HCID투입량
반응물4-Amino-1-butanolHCID 25868—
반응물3-Chloro-1,2-benzoxazoleHCID 2779780—
촉매Potassium IodideHCID 4875—
용매DichloromethaneHCID 6344—
생성물4-(1,2-Benzisoxazol-3-ylamino)-1-butanolHCID 1837895793.3%

반응 조건

온도80 °C

반응 단계

A mixture of 3-chloro-1,2-benzisoxazole (0.08 mol), 4-amino-1-butanol (0.24 mol) and potassium iodide (1 g) was stirred for 4 days at 80° C. The reaction mixture was cooled, dissolved in CH2Cl2 and purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 95/5). The pure fractions were collected and the solvent was evaporated, yielding 15.4 g (93%)of 4-(1,2-benzisoxazol-3-ylamino)-1-butanol (interm. 7). b) SOCl2 (0.048 mol) was cooled to 0° C. A solution of intermediate 7 (0.048 mol) in CHCl3 (20 ml) was added dropwise and the reaction mixture was stirred overnight at room temperature. The solvent was evaporated. The residue was washed with water. The reaction mixture was extracted with CH2Cl2. The separated organic layer was dried, filtered, and the solvent was evaporated, yielding 10.4 g of N-(4-chlorobutyl)-1,2-benzisoxazol-3-amine (interm. 8).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352999B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-a37a3a890d5242feba69af330434052b
출처 메모uspto-grants-2002_03