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p-Toluenesulfonic acid → 2,3-Dihydro-1,3-dimethyl-2-dodecylperimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Tridecanal | HCID 25311 | — |
| 反応物 | N,N'-Dimethyl-1,8-naphthalenediamine | HCID 140748 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2,3-Dihydro-1,3-dimethyl-2-dodecylperimidine | HCID 15404100 | — |
反応手順
A mixture of N,N'-dimethyl-1,8-naphthalene diamine (prepared in Example 1) (0.50 g, 2.7 mmol, 186), tridecanal (0.56 g, 2.85 mmol. 197), p-toluenesulfonic acid (5 mg), and tetrahydrofuran (5 ml) was prepared and stirred at room temperature for 15 minutes. The mixture was basified with 25% sodium hydroxide (1.0 ml), diluted with water (20 ml) and extracted with ether (100 ml). The extract was dried over potassium carbonate, concentrated to give 2,3-dihydro-1,3-dimethyl-2-dodecyl perimidine as a solid: mp 30°-32° C.; NMR (CDCl3) 7.13(m, 4H), 6.32(d, 2H), 4.27(t, 1H), 3.02(s, 6H), 1.7-1.1(m, 22H), 0.85(t, 3H); IR (neat) 1595 cm-1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05097029 |
| 出典データセット | uspto-grants-1992_03 |
| ORD ID | ord-94ad1b5147d04401a56bb19c28001f31 |
| 出典メモ | uspto-grants-1992_03 |