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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 444661생성일: 2026년 10월 25일

Hydrochloric Acid → 3,7-Dibromodibenzo(b,d)thiophene

https://huagongshe.com/reaction/444661

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl EtherHCID 3283—
반응물3,7-Dibromo-dibenzothiophene 5,5-dioxideHCID 4071898—
반응물Aluminium lithium hydrideHCID 21226445—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물3,7-Dibromodibenzo(b,d)thiopheneHCID 80375948.1%

반응 단계

In a 500-ml flask, lithium aluminum hydride (4.1 g) is slowly introduced in small amounts over 50 minutes into a mixture of 3,7-dibromodibenzothiophene dioxide (20 g) and anhydrous ether (200 ml) in an ice bath, and the resulting mixture is refluxed and stirred for 2 hours. Water (200 ml) is added thereto to deactivate lithium aluminum hydride. Chloroform (200 ml) and concentrated hydrochloric acid (40 ml) are added thereto, the mixture is thoroughly stirred, and the organic layer is separated. The aqueous layer is further extracted with chloroform (200 ml×2), the chloroform extract is combined with the organic layer, and the combined organic layer is washed with water (200 ml) and saturated brine (200 ml), and dried over calcium chloride. The solvent is distilled off, and colorless crystals thus obtained are recrystallized from ethyl acetate+ethanol (16:3). Thus, 8.8 g of 3,7-dibromodibenzothiophene is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08475984B1
출처 데이터셋uspto-grants-2013_07
ORD IDord-e8993a482e264607916821b1a435b3a0
출처 메모uspto-grants-2013_07