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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248607생성일: 2026년 10월 24일

2-Mercaptoethanol → Ethanol, 2-[[(4-ethenylphenyl)methyl]thio]-

https://huagongshe.com/ko/reaction/248607

반응식

참여 물질

역할이름HCID투입량
반응물2-MercaptoethanolHCID 1567—
반응물Potassium HydroxideHCID 14797—
반응물2,6-Di-tert-butyl-4-methylphenolHCID 31404—
반응물p-Vinylbenzyl chlorideHCID 74126—
용매EthanolHCID 702—
생성물Ethanol, 2-[[(4-ethenylphenyl)methyl]thio]-HCID 1469279885%

반응 단계

To a solution of potassium hydroxide (86 g, 1.3 moles) and 2,6-di-tert-butyl-p-cresol (1 g) in ethanol (1 liter) at room temperature was added under nitrogen atmosphere 2-mercaptoethanol (100 g, 1.3 moles), over fifteen minutes. Following addition the solution was stirred an additional hour at room temperature and then p-vinylbenzyl chloride (198 g, 1.3 moles) was added at room temperature over one hour. After addition, the mixture was allowed to reach ambient temperature overnight. The mixture was filtered and the solvent removed on a rotary evaporator. To the residue was added dichloromethane (1.2 liter) and the solvent was washed with water (3×200 ml), then with saturated NaCl solution (200 ml), dried over anhydrous magnesium sulfate, filtered and the solvent removed on a rotary evaporator. To the residue was added diethyl ether (200 ml) and petroleum ether (800 ml). The product crystallized and was then filtered to give a white solid: m.p. of 44°-45.5° C. Yield of 85%. Analysis calculated for C11H14OS: C. 68.0, H, 7.26, S, 16.50. Found: C, 67.7, H, 6.98, S, 15.37.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210289
출처 데이터셋uspto-grants-1993_05
ORD IDord-a6799965982b4b4484729b3c3149fb1c
출처 메모uspto-grants-1993_05