HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hexane → 4-Chloro-3-(3-methyl-2-butenyloxy)benzenamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 1-Chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene | HCID 12985690 | — |
| Katalysator | Iron | HCID 23925 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 4-Chloro-3-(3-methyl-2-butenyloxy)benzenamine | HCID 12985691 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06710077B1 |
| Quelldatensatz | uspto-grants-2004_03 |
| ORD ID | ord-c4e4019637dc499c97aa04611feb8ff6 |
| Quellennotiz | uspto-grants-2004_03 |