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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341673생성일: 2026년 10월 25일

Hydrochloric Acid → HCID 68733026, 화합물

https://huagongshe.com/reaction/341673

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물ChloroformHCID 6212—
반응물2,2,6,6-Tetramethylthiopyran-3,5-dioneHCID 15650165—
반응물HCID 178476529HCID 178476529—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TolueneHCID 1140—
생성물HCID 68733026HCID 6873302640.9%

반응 조건

온도80 °C

반응 단계

2,2,6,6-Tetramethylthiopyran-3,5-dione (10 g, 0.053 mol) (described in Helvetica Chimica Acta, 1992, 75(7), 2265-69) and 4-dimethylaminopyridine (32 g, 0.26 mol) are added to a mixture of chloroform (200 ml) and toluene (50 ml). The reaction mixture is flushed with nitrogen for 15 minutes at ambient temperature. 4-Bromo-2-ethylphenyllead triacetate (34 g, 0.06 mol) is added in one portion and the reaction mixture is stirred and heated to 80° C. (pre-heated oil bath) under an atmosphere of nitrogen for 1 hour. The reaction mixture is cooled to room temperature, acidified to pH 1 with 2N aqueous hydrochloric acid, filtered through a plug of diatomaceous earth and the two phases are separated. The aqueous phase is extracted with dichloromethane (2×100 ml). The organic phases are combined, washed with water, and dried over anhydrous sodium sulfate. The mixture is filtered, and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 4-(4-bromo-2-ethylphenyl)-2,2,6,6-tetramethylthiopyran-3,5-dione as a white solid (8 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895761B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-2c6339ad292648158a10cbb0d68069b5
출처 메모uspto-grants-2014_11