化工社化工社 化学情報印刷レポート · 研究参考用
Water → (4-Tert-butyl-benzyl)-(2-pyridin-4-yl-ethyl)-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| 反応物 | 4-Pyridineethanamine | HCID 83275 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (4-Tert-butyl-benzyl)-(2-pyridin-4-yl-ethyl)-amine | HCID 60913740 | 91.3% |
反応手順
1.22 g (10 mmol) of 2-(4-pyridyl)-ethyl amine and 1.62 g (10 mmol) of 4-tert-butyl benzaldehyde were dissolved in 20 ml methanol and stirred at rt over night. 555 mg (15 mmol) of sodium borohydride were added in portions under cooling. After complete addition the reaction mixture was stirred for 1 h at rt. Water was added and methanol was evaporated. The reaction mixture was extracted twice with diethyl ether. The combined organic layers were washed with water, dried over sodium sulfate, filtered and the solvent was evaporated to yield 2.45 g (91%) product as a light yellow oil. 1H NMR (DMSO-d6, 300 MHz): δ 8.49 (d, 2H), 7.34 (d, 2H) 7.21 (d, 2H), 7.13 (d, 2H), 3.77 (s, 2H), 2.93 (t, 2H), 2.81 (t, 2H), 1.31 (s, 9H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07259183B2 |
| 出典データセット | uspto-grants-2007_08 |
| ORD ID | ord-e242a4347b414e95a8e96bf70343bff4 |
| 出典メモ | uspto-grants-2007_08 |