HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethanol → 3-(3-Bromo-phenoxymethyl)-phenylamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 1-Nitro-3-(3-bromo-phenoxymethyl)-benzene | HCID 28369541 | — |
| Katalysator | Iron | HCID 23925 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-(3-Bromo-phenoxymethyl)-phenylamine | HCID 20112959 | 97% |
Reaktionsschritte
To a solution of the product from Example 104A (1.64 g, 5.32 mmol), iron powder (1.49 g, 26.62 mmol) and ammonium chloride (430 mg, 7.98 mmol) in a mixture of tetrahydrofuran (20 mL), water (6 mL) and ethanol (20 mL) was heated to reflux for 3 hours. The mixture was cooled to room temperature, filtered through a pad of celite, which was washed with ethanol and the resultant filtrate concentrated under vacuum. The material was then dissolved in water (50 mL) and extracted with ethyl acetate (50 mL), the organic layer dried and concentrated under vacuum to provide the title compound as a yellow oil (1.43 g, 97%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07915411B2 |
| Quelldatensatz | uspto-grants-2011_03 |
| ORD ID | ord-cba2877cacb1487c83615460cf0ad156 |
| Quellennotiz | uspto-grants-2011_03 |