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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1815942생성일: 2026년 10월 26일

Propylene Oxide → (6-Benzyloxy-indol-1-yl)-propan-2-ol

https://huagongshe.com/reaction/1815942

반응식

참여 물질

역할이름HCID투입량
반응물Propylene OxideHCID 6378—
반응물Sodium hydrideHCID 24758—
반응물6-(benzyloxy)-1H-indoleHCID 260804—
반응물Monobasic potassium phosphateHCID 516951—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(6-Benzyloxy-indol-1-yl)-propan-2-olHCID 22247173—

반응 단계

To a stirred, cooled (10° C.) suspension of sodium hydride (80.7 g of a 60% dispersion in mineral oil, 2.02 mol) in anhydrous THF (1.9 L) was added a solution of 6-benzyloxyindole (375 g, 1.68 mol) in anhydrous THF (1.9 L) keeping the temperature below 25° C. After 2 h at 10° C., propylene oxide (140 mL, 2.0 mol) was added dropwise keeping the temperature below 25° C. After 48 h at 10° C., propylene oxide (71 mL, 1.0 mol) was added. After 96 h at 10° C., saturated aqueous potassium dihydrogenphosphate (3.8 L) and ethyl acetate (3.8 L) were carefully added, the layers were separated and the aqueous solution was extracted with 3.8 L of ethyl acetate. The combined organic extracts were dried over sodium sulfate and concentrated in vacuo to yield a solid (520 g, 110%, contains mineral oil).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06881749B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-432474aceda8463f84b8e7c88480f53e
출처 메모uspto-grants-2005_04