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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62269생성일: 2026년 10월 24일

p-Toluenesulfonic acid → (E)-5-bromo-6-methoxy-2-(3-(trifluoromethyl)benzylidene)-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/ko/reaction/62269

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물3-(Trifluoromethyl)benzaldehydeHCID 67990—
반응물5-Bromo-6-methoxy-1-indanoneHCID 22278718—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물(E)-5-bromo-6-methoxy-2-(3-(trifluoromethyl)benzylidene)-2,3-dihydro-1H-inden-1-oneHCID 117940380—

반응 조건

온도120 °C

반응 단계

A solution of 11 (200 mg, 0.829 mmol) in toluene was added 3-(trifluoromethyl)benzaldehyde 99 (158.86 mg, 0.9128 mmol). PTSA (285.5 mg, 172.20 mmol) was added to the reaction mass. The reaction was stirred at 120° C. for 6 h. The reaction mass was diluted with ethyl acetate and washed with water (3×25 mL). The organic layer was dried over sodium sulphate and concentrated to get the crude compound 152 which was purified through flash chromatography by using 100-200 mesh silica gel. The compound (E)-5-bromo-6-methoxy-2-(3-(trifluoromethyl)benzylidene)-2,3-dihydro-1H-inden-1-one 152 was eluted at 30% ethyl acetate in hexane to afford yellow coloured solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09446047B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-ea18cb7f2a904ee09949cf7bbf975182
출처 메모uspto-grants-2016_09