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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15402생성일: 2026년 10월 25일

Water → (2-Bromophenylthiomethyl)-1,3-dioxolane

https://huagongshe.com/reaction/15402

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
반응물2-BromobenzenethiolHCID 80598—
용매DimethylformamideHCID 6228—
생성물(2-Bromophenylthiomethyl)-1,3-dioxolaneHCID 23156709—

반응 단계

To a mixture of 2-bromothiophenol (5 g) and 2-bromomethyl-1,3-dioxolane (2.98 mL) in N,N-dimethylformamide (50 mL) was added potassium carbonate (5.48 g) at room temperature, and the mixture was stirred overnight. The reaction mixture was poured into water, and the mixture was extracted with diethyl ether. The extract washed with water, 1 mol/L sodium hydroxide aqueous solution, water and brine successively, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to give (2-bromophenylthiomethyl)-1,3-dioxolane (7.25 g). To a mixture of poly phosphoric acid (20 g) and chlorobenzene (40 mL) was added a solution of (2-bromophenylthiomethyl)-1,3-dioxolene (7.25 g) in chlorobenzene (20 mL), and the mixture was refluxed for 8 hours. The reaction mixture was cooled to room temperature and supernatant solution was collected by decantation. Toluene was added to the residue, and the supernatant was collected by decantation after the mixture was stirred. The supernatant was combined and concentrated under reduced pressure. The residue was dissolved in ethyl acetate, and the solution washed with a saturated sodium hydrogencarbonate aqueous solution, water and brine and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: n-hexane) to give the title compound (2.27 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732596B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-8b0b2d96e28c43b7a9b254da7adc77a8
출처 메모uspto-grants-2010_06