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Piperidine → 2-[4-(Diethylamino)styryl]-1-hexylpyridinium bromide hemihydrate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 4-(Diethylamino)benzaldehyde | HCID 67114 | — |
| 反応物 | 1-Hexyl-2-methylpyridinium bromide | HCID 21987866 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-[4-(Diethylamino)styryl]-1-hexylpyridinium bromide hemihydrate | HCID 70455364 | 45.3% |
反応手順
1-Hexyl-2-methylpyridinium bromide (7.8 g, 0.03 mole) and 4-diethylaminobenzaldehyde (7.0 g, 0.04 mole) were refluxed in methanol (50 ml) in the presence of piperidine (1.0 ml) under nitrogen for four hours. The solution was evaporated and the resulting oil was redissolved in a small amount of isopropanol. Addition of twice the volume of ether gave a red crystalline solid which was collected and washed with isopropanol/ether to give 2-[4-(diethylamino)styryl]-1-hexylpyridinium bromide hemihydrate (5.8 g), melting point 222°-223° (decomposition).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04608379 |
| 出典データセット | uspto-grants-1986_08 |
| ORD ID | ord-309cd08193b94334b1b909faff8e5a58 |
| 出典メモ | uspto-grants-1986_08 |