Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 5-(Benzyloxy)-2,3-dihydro-1H-indole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 5-Benzyloxyindole | HCID 14624 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 5-(Benzyloxy)-2,3-dihydro-1H-indole | HCID 16794881 | 89.2% |
반응 단계
In analogy to the method described by Gordon W. Gribble, Joseph H. Hoffmann Synthesis 1977, 859-860, the following reaction was performed. To a precooled solution of 22.3 g (0.1 mol) 5-benzyloxyindole in 270 ml acetic acid, 19 g (0.3 mol) NaCNBH3 were added. The solution was stirred at RT for 2 h, the volume was reduced to one third and poured into 300 ml water. KOH was added under cooling and the solution was extracted with ether. The combined organic phases were washed with water, dried over Na2SO4 and evaporated to yield 20.1 g (89%) 5-Benzyloxy-2,3-dihydro-1H-indole as colorless oil, MS: 225 (M).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06706751B2 |
| 출처 데이터셋 | uspto-grants-2004_03 |
| ORD ID | ord-bd86c4538ce548e0b9203acfa8be0660 |
| 출처 메모 | uspto-grants-2004_03 |