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Ethanol → 2-chloro-1H-indole-3-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 2-chloro-1H-indole-3-carbaldehyde | HCID 314791 | — |
| 反応物 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Acetic Anhydride | HCID 7918 | — |
| 生成物 | 2-chloro-1H-indole-3-carbonitrile | HCID 10329854 | 58% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05464861 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-3e3748a6eb08424ebcc6169c3886b319 |
| 出典メモ | uspto-grants-1995_11 |