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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253711생성일: 2026년 10월 26일

Methanol → 2-[2-(Diethylamino)ethylthio]ethanol

https://huagongshe.com/reaction/253711

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물2-BromoethanolHCID 10898—
반응물Sodium HydroxideHCID 14798—
반응물Ethanethiol, 2-(diethylamino)-, hydrochloride (1:1)HCID 16031—
용매WaterHCID 962—
생성물2-[2-(Diethylamino)ethylthio]ethanolHCID 525654587.5%

반응 단계

2-(Diethylamino)ethanethiol hydrochloride (5.0 g, 29 mmol) was added to a 250 mL round-bottom flask, 20 mL methanol was added, and the solution cooled in an ice bath with stirring. Sodium hydroxide (2.34 g, 58 mmol), dissolved in water (15 mL), was added, followed by slow addition of 2-bromoethanol (5.9 g, 47 mmol). Stirring was continued while the reaction mixture was allowed to warm to room temperature overnight. The methanol and water were removed under reduced pressure, and the residue dissolved in ethyl acetate (100 mL), washed with water (3×20 mL), dried over magnesium sulfate, and concentrated under reduced pressure to give 2-[2-(diethylamino)-ethylthio]ethanol as a yellow oil (4.5 g, 87% yield). LC-MS (ES+): m/z=178 [C8H19NOS+H+] for product peak. A 1.0 g aliquot of the crude 2-[2-(diethylamino)ethylthio]ethanol was purified by flash chromatography on silica cartridges, eluting with a gradient of 100% hexane to 100% ethyl acetate over 5 minutes, to give 0.78 g pure 2-[2-(diethylamino)ethylthio]ethanol as a colorless oil after evaporation of the solvents, and the remaining 3.5 g similarly purified, eluting with a gradient of 100% hexane to 100% ethyl acetate over 20 minutes, to give an additional 3.11 g pure 2-[2-(diethylamino)ethylthio]ethanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872134B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-79ac0a73b45b4a6280ffe1b1e6eb3d21
출처 메모uspto-grants-2011_01