Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434020생성일: 2026년 10월 26일
Sodium hydride → 5-Allyloxy-1-[(6-chlorobenzo[1,3]dioxol-5-yl)methyl]-1h-indole-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/434020
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 6-Chloropiperonyl chloride | HCID 90113 | — |
| 반응물 | Ethyl 5-[(prop-2-en-1-yl)oxy]-1H-indole-2-carboxylate | HCID 13286893 | — |
| 촉매 | Tetrabutylammonium Iodide | HCID 67553 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 5-Allyloxy-1-[(6-chlorobenzo[1,3]dioxol-5-yl)methyl]-1h-indole-2-carboxylic acid ethyl ester | HCID 70032910 | 43% |
반응 단계
To a mixture of NaH (60% suspension in mineral oil, 0.24 g, 6.12 mmol) and DMF (20 mL) was added 5-allyloxyindole-2-carboxylic acid ethyl ester (1.0 g, 4.08 mmol), from Example 1(d). After stirring at room temperature for 1 h, 6-chloropiperonyl chloride (0.84 g, 4.08 mmol) was added followed by the addition of tetrabutyl ammonium iodide (0.15 g, 0.41 mmol). The reaction was stirred at room temperature for 18 h. When the reaction was complete as indicated by TLC, the reaction mixture was partitioned between EtOAc and water. The organic layer was washed with brine and dried (Na2SO4). The solvent was removed in vacuo and the resulting crude product was purified by flash column chromatography (silica gel, EtOAc/hexanes) to yield the desired product as an oil (0.72 g, 43%). LC/MS (ES+) m/e 414.0 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06670388B1 |
|---|
| 출처 데이터셋 | uspto-grants-2003_12 |
|---|
| ORD ID | ord-b1232f5cd63a4771b76d4c4fa67413d4 |
|---|
| 출처 메모 | uspto-grants-2003_12 |
|---|