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HRID 248607作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-MercaptoethanolHCID 1567—
反応物Potassium HydroxideHCID 14797—
反応物2,6-Di-tert-butyl-4-methylphenolHCID 31404—
反応物p-Vinylbenzyl chlorideHCID 74126—
溶媒EthanolHCID 702—
生成物Ethanol, 2-[[(4-ethenylphenyl)methyl]thio]-HCID 1469279885%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05210289
出典データセットuspto-grants-1993_05
ORD IDord-a6799965982b4b4484729b3c3149fb1c
出典メモuspto-grants-1993_05