化工社化工社 化学情報印刷レポート · 研究参考用
Water → 6-Nitro-4-(2-(4-tert-butylphenyl)ethoxy)quinazoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | p-tert-Butylphenethyl alcohol | HCID 79410 | — |
| 反応物 | 4-Chloro-6-nitroquinazoline | HCID 11356257 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 6-Nitro-4-(2-(4-tert-butylphenyl)ethoxy)quinazoline | HCID 59678659 | — |
反応手順
2-(4-tert-butylphenyl)ethanol (1.0 g, 5.59 mmol) is dissolved in dry tetrahydrofuran (7 ml) and to it is added sodium hydride (48.5 mg, 2.02 mmol). The resulting solution is stirred at room temperature for 30 minutes after which 6-Nitro-4-chloroquinazoline (1.17 g, 5.6 mmol) is added to the above solution. The solution is then stirred for 6 hours after which water is added to the mixture. The solution is then extracted in dichloromethane. The organic layer is washed, dried and then concentrated to yield the crude product which is purified by flash chromatography (silica gel; ethyl acetate/hexanes) to give the product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09161997B2 |
| 出典データセット | uspto-grants-2015_10 |
| ORD ID | ord-568ea2259ee1470483cc5ba94df42635 |
| 出典メモ | uspto-grants-2015_10 |