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2-Hydroxy-1-naphthaldehyde → 2-Cyano-3-(2-hydroxynaphth-1-yl) thioacrylamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Hydroxy-1-naphthaldehyde | HCID 12819 | — |
| 反応物 | 2-Cyanoethanethioamide | HCID 1416277 | — |
| 反応物 | 1-(Diethylamino)ethanol | HCID 15894840 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-Cyano-3-(2-hydroxynaphth-1-yl) thioacrylamide | HCID 136153472 | 85% |
反応手順
A mixture of 2-hydroxy-1-naphthaldehyde (172 mg, 1 mmol), 2-cyanothioacetamide (110 mg, 1.1 mmol), N,N-diethylaminoethanol (23 mg, 0.2 mmol) and 15 ml ethanol is stirred for 30 min at reflux under nitrogen. Then the mixture is chilled, the precipitate filtered, washed with ice-cooled ethanol and dried in a vacuum-oven. Thus an almost pure title compound is obtained in 85% yield (1080 mg). Recrystallization from ethanol furnishes very pure samples.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05488057 |
| 出典データセット | uspto-grants-1996_01 |
| ORD ID | ord-3668e06acc7d4dadb904439418140511 |
| 出典メモ | uspto-grants-1996_01 |