Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzene, 1-chloro-4-fluoro- → 5-allyloxy-N-(4-chlorophenyl)indole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzene, 1-chloro-4-fluoro- | HCID 9604 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 5-(prop-2-en-1-yloxy)-1H-indole | HCID 14239230 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-allyloxy-N-(4-chlorophenyl)indole | HCID 54410488 | — |
반응 단계
To a solution of sodium hydride (60%, 254 mg, 6.35 mmol) in 15 mL tetrahydrofuran (THF) was added 5-allyloxyindole (Step A; 1.0 g, 5.77 mmol) in 5 mL THF and the mixture was stirred for 1 hour at ambient temperature. 4-fluorochlorobenzene (0.69 mL, 6.35 mmol) was added and the reaction heated to reflux for 21 hours. After cooling, the reaction was quenched with saturated aqueous ammonium chloride and extracted with ethyl acetate. The organic layer was washed with water, brine, dried over magnesium sulfate, filtered, concentrated in vacuo, and the crude residue purified by flash chromatography on silica gel (15% ethyl acetate/hexane) to provide the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05859051 |
| 출처 데이터셋 | uspto-grants-1999_01 |
| ORD ID | ord-795c175dcce247b2aacf26afcf06a6ac |
| 출처 메모 | uspto-grants-1999_01 |