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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662902생성일: 2026년 10월 24일

Triethylamine → 2-Methanesulfonyloxyethyl disulfide

https://huagongshe.com/ko/reaction/1662902

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Hydroxyethyl disulfideHCID 15906—
반응물Methanesulfonyl chlorideHCID 31297—
용매Ethyl AcetateHCID 8857—
생성물2-Methanesulfonyloxyethyl disulfideHCID 23117209—

반응 단계

10 g of 2,2′-dithiodiethanol and 14.44 g of triethylamine (TEA) are diluted in 100 mL of ethyl acetate (EtOAc). At 0° C., 16.35 g of methanesulfonyl chloride diluted in 35 mL of EtOAc are added dropwise to the reaction medium with rapid stirring. 7.22 g of TEA are introduced and stirring is continued at room temperature for 4 hours 30 minutes. 8.2 g of methanesulfonyl chloride are added dropwise at 15° C. and stirring is continued at room temperature for 17 hours. The precipitate is filtered off and washed with three times 50 mL of EtOAc. The organic phases are extracted with 100 mL of ice-water, 100 mL of water, three times 50 mL of saturated sodium hydrogen carbonate solution (NaHCO3), twice 20 mL of saturated sodium chloride solution (NaCl), and then dried over anhydrous sodium sulfate (Na2SO4). The EtOAc is evaporated off, and 17.49 g of a clear pale yellow oil are collected and stored at −25° C. The analyses indicate that the product is in accordance and pure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08034125B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-d22e9669e8ec46ab922a0eafd7764b81
출처 메모uspto-grants-2011_10