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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6429생성일: 2026년 10월 23일

2-Aminophenol → 2-(2H-Pyrrol-2-ylidene)-2,3-dihydro-1,3-benzoxazole

https://huagongshe.com/ko/reaction/6429

반응식

참여 물질

역할이름HCID투입량
반응물2-AminophenolHCID 5801—
반응물Boric AcidHCID 7628—
반응물Pyrrole-2-Carboxylic AcidHCID 12473—
용매O-XyleneHCID 7237—
용매Ethyl AcetateHCID 8857—
생성물2-(2H-Pyrrol-2-ylidene)-2,3-dihydro-1,3-benzoxazoleHCID 13562548252%

반응 단계

2-(Pyrrol-2-yl)benzoxazole was prepared as follows: A mixture of 5.55 g (0.05 mol) of pyrrole-2-carboxylic acid and 5.46 g (0.05 mol) of o-aminophenol and 3.09 g (0.05 mol) boric acid in 50 mL of xylene was heated under reflux for 3 days while removing water which was generated from reaction using a Dean-Stark trap. The cooled reaction mixture was diluted with 100 mL of ethyl acetate, washed with 150 mL of 5% sodium hydroxide solution and then with 150 mL of water. The separated organic layer was dried over anhydrous sodium sulfate. The resulting crude product was purified by column chromatography on silica gel with 20% hexane in chloroform as eluant. The desired product, 2-(pyrrol-2-yl)benzoxazole (4.75 g, 52%), was obtained as a white solid. m.p. 149°-150° C.; 1H NMR (CDCl3) δ6.38-6.40 (m, 1H, ArH), 7.05-7.06 (m, 1H, ArH), 7.11-7.13 (m, 1H, ArH), 7.29-7.36 (m, 2H, 2xArH), 7.53-7.56 (m, 1H, ArH), 7.65-7.69 (m, 1H, ArH), 10.9 (bs, 1H, NH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248782
출처 데이터셋uspto-grants-1993_09
ORD IDord-2288569fc3ee4fffb9e3876b2052db84
출처 메모uspto-grants-1993_09