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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15239생성일: 2026년 10월 24일

Oxygen → 4-Hydroxydibenzothiophene

https://huagongshe.com/ko/reaction/15239

반응식

참여 물질

역할이름HCID투입량
반응물OxygenHCID 977—
반응물DibenzothiopheneHCID 3023—
반응물HCID 178418306HCID 178418306—
반응물HCID 178418443HCID 178418443—
용매TetrahydrofuranHCID 8028—
생성물4-HydroxydibenzothiopheneHCID 15487396%

반응 조건

온도-78 °C

반응 단계

To a cooled (−78° C.) solution of dibenzothiophene (20.8 g, 113 mmol) in anhydrous THF (400 ml) was added tert-butyl lithium (1.7 M in pentane; 100 ml, 170 mmol). The reaction mixture was stirred at −78° C. for 1 hour and then allowed to warm to room temperature and stirred like this for 16 hours. The mixture was then cooled to 0° C. and ethylmagnesium bromide (1M in THF; 170 ml, 170 mmol) added to the amber reaction mixture in a slow stream via cannula. The reaction was again allowed to room temperature whereupon it was stirred like this for 30 minutes. A reflux condenser was attached to the reaction vessel before oxygen was bubbled through the solution for 40 minutes. The mixture was then stirred for a further 1 hour before carefully pouring onto crushed ice and acidifying to pH 3 with concentrated HCl. The mixture was then extracted using ethyl acetate (3×80 ml). The organic extracts were then treated with 3M sodium hydroxide solution until pH 10 was attained. The basic, aqueous layer was separated, acidified to pH 3 with 2M HCl which caused an oily solid to precipitate. This was dissolved in diethylether (150 ml), dried using MgSO4, filtered and concentrated in vacuo and then recrystallised from ethanol:water (1:1) (250 ml) to give a buff coloured solid that corresponded to the title compound (21.6 g, 96%) and required no further purification. m/z (LC-MS, ESP), RT=3.64 min, (M+H)=201.1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732483B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-33f19fa137be4af5abf47f0b8cd81b05
출처 메모uspto-grants-2010_06