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Dimethylformamide → 3-[2-(Dimethylamino)ethenyl]pyridine-2-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 3-Methylpyridine-2-carbonitrile | HCID 819928 | — |
| 生成物 | 3-[2-(Dimethylamino)ethenyl]pyridine-2-carbonitrile | HCID 53713307 | 56% |
反応手順
A solution of 3-methyl-2-cyanopyridine (20.0 g, 0.17 m), DMF (200 mL) and DMF acetal (30 mL, 0.25 m) was heated at 120° with stirring under N2 for 5 days. Additional acetal was periodically added in 5 mL aliquots (total 45 mL, 0.38 m). The solution was then evaporated to dryness to give a crude oil which solidified on standing. The solid was crystallized from ligroin to yield 16.5 g (56%) of N,N-dimethyl-2-(2-cyano-3-pyridyl)ethenamine. An analytical sample was prepared by recrystallization from ligroin, mp 71.5°-72°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04176183 |
| 出典データセット | uspto-grants-1979_11 |
| ORD ID | ord-9b7b082db0304f9b872f64baf33f2cfb |
| 出典メモ | uspto-grants-1979_11 |