化工社化工社 化学情報印刷レポート · 研究参考用
Hexane → 4-Chloro-3-(3-methyl-2-butenyloxy)benzenamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | 1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene | HCID 12985690 | — |
| 触媒 | Iron | HCID 23925 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 4-Chloro-3-(3-methyl-2-butenyloxy)benzenamine | HCID 12985691 | — |
反応手順
To a refluxing well-stirred suspension of iron powder (19.6 g, 100 mesh) in ethanol (60 mL), water (13.4 mL) and 36% hydrochloric acid (1.4 mL) was added 1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene (24 g) in portions over 15-30 minutes. After 3 hours thin-layer chromatography (TLC) (ethyl acetate:hexane, 40:60) showed no substrate. The reaction mixture was then filtered hot and the iron oxide filter cake was washed with hot ethanol. The combined ethanol washes were evaporated to produce a residue. The residue was taken up in diethyl ether, washed with aqueous bicarbonate and water, dried (MgSO4), filtered, and evaporated, to give 4-chloro-3-(3-methyl-2-butenyloxy)benzenamine, 19.8 g of light brown oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06710077B1 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-c4e4019637dc499c97aa04611feb8ff6 |
| 出典メモ | uspto-grants-2004_03 |