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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327659생성일: 2026년 10월 24일

Triethylamine → 3-Phenoxy-1,2-propanediol bissulfamate

https://huagongshe.com/ko/reaction/327659

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Phenoxy-1,2-propanediolHCID 10857—
반응물Chlorosulfamic acidHCID 24499—
용매AcetonitrileHCID 6342—
생성물3-Phenoxy-1,2-propanediol bissulfamateHCID 54339921—

반응 단계

To the above sulfamoyl chloride solution in acetonitrile was added dropwise with stirring a solution of 8.4 g (0.05 mole) of 3-phenoxy-1,2-propanediol (95% purity obtained from Aldrich Chem. Co., Inc.) and 20.2 g (0.2 mole) of triethylamine in 50 ml of acetonitrile at such a rate that the temperature did not exceed 12° C. over a 45 min period. The cooling bath was removed and the mixture was stirred for 2 hr and treated with 100 ml of ethyl acetate and 50 ml of water. The mixture was vigorously stirred for 5 min and the layers were separated. The organic layer was washed with 50 ml of water and 100 ml of salt brine, dried over sodium sulfate and concentrated to give a gum as residue. The gum was purified by column chromatography on 350 g of silica gel. Fractions eluted with 15% acetone in methylene chloride were combined and concentrated to give a clear gum as residue. The gum was triturated with petroleum ether (b.p. 30°-60° C.) to give crystalline solid. The solid was collected by filtration and recrystallized from benzene-acetonitrile to yield 4.2 g (26% yield) of white solid title compound, mp 116°-118° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05273993
출처 데이터셋uspto-grants-1993_12
ORD IDord-b9c81e9390394da5888ee64452b6444a
출처 메모uspto-grants-1993_12