Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethanol → 2-chloro-1H-indole-3-carbonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | 2-chloro-1H-indole-3-carbaldehyde | HCID 314791 | — |
| 반응물 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Acetic Anhydride | HCID 7918 | — |
| 생성물 | 2-chloro-1H-indole-3-carbonitrile | HCID 10329854 | 58% |
반응 단계
A mixture of 2-chloroindole-3-carboxaldehyde (7.0 g, 36 mmol) was reacted with a slight excess of hydroxylamine hydrochloride and pyridine in refluxing EtOH for 1 hour, to give the crude oxime (Latrell R, Bartmann W, Musif J, Granzer E, German Patent 2,707,268, 31 Aug 1978, Chem. Abstr. 1978;89:179858y). A solution of this in Ac2O (100 mL) was heated under reflux for 1 hour, cooled, and stirred with water (700 mL). The precipitated solid was collected, washed with water, and crystallized from aqueous MeOH to give 2-chloro-1H-indole-3-carbonitrile (3.7 g, 58%); mp 177°-180° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05464861 |
| 출처 데이터셋 | uspto-grants-1995_11 |
| ORD ID | ord-3e3748a6eb08424ebcc6169c3886b319 |
| 출처 메모 | uspto-grants-1995_11 |