Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethanol → 6-Iodoindoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 1-Acetyl-6-iodoindoline | HCID 11666396 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 6-Iodoindoline | HCID 11615696 | 64% |
반응 단계
1-Acetyl-6-iodoindoline (1.06 g, 3.7 mmol), NaOH (1.16 g, 29 mmol), EtOH (8 mL), and H2O (6 mL) are heated at 90° C. overnight. The reaction mixture is then partitioned between H2O and EtOAc. The organic layer is extracted into aqueous HCl. The aqueous layer is in turn basified with NaOH, and is extracted with EtOAc. The organic layer is dried and concentrated. Hexane trituration yields 6-iodoindoline (577 mg, 64%) as a brown solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07973069B2 |
| 출처 데이터셋 | uspto-grants-2011_07 |
| ORD ID | ord-39c37c3b0c3d45a8b01105da888629fe |
| 출처 메모 | uspto-grants-2011_07 |