HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 1-[4-(4-Aminobutoxy)phenyl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 2-[4-(4-Acetylphenoxy)butyl]-1H-isoindole-1,3(2H)-dione | HCID 67598087 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[4-(4-Aminobutoxy)phenyl]ethanone | HCID 53857985 | — |
Reaction Steps
A suspension of 13.5 g of 2-[4-(4-acetyl-phenoxy)butyl]-1H-isoindole-1,3(2H)-dione in 500 ml of ethanol is treated with 1.4 ml of anhydrous hydrazine, and the mixture stirred at reflux for 9 hours. After cooling to room temperature, the precipitate is collected. Concentration of the filtrate gives the crude title compound, which is used directly for further synthesis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05877196 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-6cbea0b89fcd4d0aaed11e41adb43517 |
| Source note | uspto-grants-1999_03 |