Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzenesulfonyl chloride → 1-benzenesulfonyl-3-bromo-6-nitro-1H-indole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzenesulfonyl chloride | HCID 7369 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3-Bromo-6-nitro-1H-indole | HCID 14707934 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-benzenesulfonyl-3-bromo-6-nitro-1H-indole | HCID 57442196 | 76.5% |
반응 단계
Sodium hydride (461 mg, 11.5 mmol) was slowly added to a solution of 3-bromo-6-nitro-1H-indole (2.32 g, 9.61 mmol) in tetrahydrofuran (10.0 mL). After stirring for 5 min, benzenesulfonyl chloride (1.47 mL, 11.5 mmol) was added dropwise over 10 min. The reaction was stirred an additional 1.5 h before quenching with 5.0 mL of methanol, followed by 10.0 mL water and 20.0 mL methylene chloride. The precipitate was filtered off and washed with an excess of methylene chloride and methanol to give a crème-colored powder for 3-bromo-6-nitro-1-(phenylsulfonyl)-1H-indole (2.80 g, 7.35 mmol, 76%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09144557B2 |
| 출처 데이터셋 | uspto-grants-2015_09 |
| ORD ID | ord-61e947e1665143c7be2c4f5506605dfa |
| 출처 메모 | uspto-grants-2015_09 |