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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36089생성일: 2026년 10월 23일

Water → 5,8-Dihydro-1,4-naphthoquinone

https://huagongshe.com/ko/reaction/36089

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물QuinoneHCID 4650—
반응물1,3-ButadieneHCID 7845—
용매Acetic AcidHCID 176—
용매TolueneHCID 1140—
생성물5,8-Dihydro-1,4-naphthoquinoneHCID 22381391%

반응 단계

In toluene (30 ml) and acetic acid (10 ml), were dissolved 10.0 g (0.092 mol) of 1,4-benzoquinone, to which 10.0 g (0.18 mol) of 1,3-butadiene were added at -10° C. under stirring. Thereafter, the resultant mixture was gradually heated and stirred further for 3 hours at 40° C. The liquid reaction mixture was washed with water, and an organic layer was dried and concentrated under reduced pressure. Concentrated hydrochloric acid (1 ml) and ethanol (50 ml) were added to the residue, and the mixture was stirred for 1 hour at 40° C. After the liquid reaction mixture was concentrated under reduced pressure, the residue was dissolved in a liquid mixture of acetonitrile (100 ml) and water (30 ml). To the solution, were added 20.0 g (0.036 mol) of ceric ammonium nitrate at room temperature to stir the resultant mixture for 1 hour. The liquid reaction mixture was poured into water (200 ml) to make extraction with toluene (50 ml × 2). The resulting organic layer was washed with water, dried and concentrated under reduced pressure to obtain 13.3 g of a crude product of the title compound (yield: 91%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05412124
출처 데이터셋uspto-grants-1995_05
ORD IDord-977f78c9e987497bad643853aae1b4fe
출처 메모uspto-grants-1995_05