HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[2-(9-anthryloxy)ethyl]phthalimide → Ammonium Hydroxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[2-(9-anthryloxy)ethyl]phthalimide | HCID 14373233 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | 1-(9-Anthryloxy)-2-aminoethane | HCID 14373234 | — |
Reaction Steps
N-[2-(9-anthryloxy)ethyl]phthalimide (6.5 g) was refluxed for 3 hours in ethanol containing 85% hydrazine hydrate (3.0 ml). The solution was cooled and diluted with ethyl acetate. The resultant solution was washed with dilute aqueous potassium hydroxide, dried and evaporated. The crude product was chromatographed on 300 g silica gel, eluting with a solution of methylene chloride:methanol:ammonium hydroxide, 95:4:1, yielding 1-(9-anthryloxy)-2-aminoethane, which was converted to the maleate, mp 190°-195° C., according to the method of Example 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04792551 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-e0ad50f2f3474ce98cbd9698019241a7 |
| Source note | uspto-grants-1988_12 |