참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Propylene Oxide | HCID 6378 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 6-(benzyloxy)-1H-indole | HCID 260804 | — |
| 반응물 | Monobasic potassium phosphate | HCID 516951 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (6-Benzyloxy-indol-1-yl)-propan-2-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06881749B2 |
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| 출처 데이터셋 | uspto-grants-2005_04 |
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| ORD ID | ord-432474aceda8463f84b8e7c88480f53e |
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| 출처 메모 | uspto-grants-2005_04 |
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