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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248609생성일: 2026년 10월 26일

2-Bromoethanol → 2-{2-[2-(4-Vinylbenzylthio)ethoxy]ethylthio}ethanol

https://huagongshe.com/reaction/248609

반응식

참여 물질

역할이름HCID투입량
반응물2-BromoethanolHCID 10898—
반응물Potassium HydroxideHCID 14797—
반응물p-Vinylbenzyl chlorideHCID 74126—
반응물2,2'-OxybisethanethiolHCID 75073—
용매EthanolHCID 702—
생성물2-{2-[2-(4-Vinylbenzylthio)ethoxy]ethylthio}ethanolHCID 1910544243.7%

반응 단계

To a solution of potassium hydroxide (48 g, 0.72 molar) in ethanol (1 liter) was added bis(2-mercaptoethyl)ether (100 g, 0.72 moles) and the mixture was stirred for 30 minutes at ambient temperature. Then 2-bromoethanol (90 g, 0.72 mole) was added to the mixture all at once and stirring was continued at ambient temperature for 30 minutes, then potassium hydroxide (48.0 g, 0.72 mole) was added to the mixture and again stirring was continued at ambient temperature for 30 minutes. p-Vinylbenzyl chloride (110 g, 0.72 mole) was then added all at once and stirred at room temperature for 16 hours. The next day the reaction was filtered and the solvent removed on a rotary evaporator. To the residue was added dichloromethane (1.2 liter), the mixture was washed with water (200 ml), 5% hydrochloric acid (200 ml), saturated sodium chloride (200 ml) then dried over anhydrous magnesium sulfate, filtered and the solvent removed in a rotary evaporator. To the residue was added diethyl ether (350 ml) and hexane (200 ml) and then the mixture was cooled in the freezer, filtered to give a white solid (94 g). Chromatography on the mother liquors gave additional product (48 g). Yield of 66%. Analysis calculated for C15H22O2S2. C, 60.36, H, 7.43, S, 21.49. Found: C, 60.41, H, 7.43, S, 21.14. 1H NMR (CDCl3) δ 2.7 (m, 6H, CH2S--CH2 +SCH2), 3.0-3.8 (m, 9H, ArCH2S, CH2OCH2,CH2OH), 5.15+5.65 (AB quartet, 2H, CH2 =), 6.68 (m, 1H, CH=), 7.25 (m, 4H, ArH's).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210289
출처 데이터셋uspto-grants-1993_05
ORD IDord-75f782c23277485b8f5164ad6538ce91
출처 메모uspto-grants-1993_05