돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250212생성일: 2026년 10월 27일

2-Aminophenol → 2-Aminobenzoxazole

https://huagongshe.com/reaction/250212

반응식

참여 물질

역할이름HCID투입량
반응물2-AminophenolHCID 5801—
반응물Ethyl AcetateHCID 8857—
반응물Cyanogen BromideHCID 10476—
반응물Sodium HydroxideHCID 14798—
용매WaterHCID 962—
생성물2-AminobenzoxazoleHCID 2070788.2%

반응 조건

온도45 °C

반응 단계

A mixture of 2.5 g 2-aminophenol (7-1) and 20 ml ethyl acetate was heated to 45° C. 3 g of cyanogen bromide was added to the mixture. The mixture was stirred at 45-50° C. for 12 hours. After cooling to room temperature, 1.5 g of sodium hydroxide in 15 ml of water was added. The organic layer was separated and washed with brine until neutral pH. Toluene (5 ml) was added and the solvent was removed to yield 2.71 g (88%) 2-aminobenzoxazol (7-2). 7.5 ml of chlorosulfonic acid was stirred at room temperature under an inert atmosphere (nitrogen). 5 g of 2-aminobenzoxazol (7-2) was added in small portions. The temperature was kept between 30-60° C. during the addition of 7-2. The mixture was heated to 80° C. for 2 hours. 5.3 g of thionyl chloride was added drop wise, keeping the temperature at 65° C. The mixture was stirred during 2 hours. After cooling to 0° C. 10 ml of ethyl acetate and 10 ml of a solution of sodium carbonate (1N) were added. The organic layer was separated from the water layer and this latter was extracted with ethyl acetate. The combined organic layers were dried over calcium chloride, yielding 7.8 g (90%) of 2-amino-6-chlorosulfonylbenzoxazole (7-3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863306B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-2c0147393f5b41559bf904db7767fd3e
출처 메모uspto-grants-2011_01