HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Acetyl-1-(p-aminophenyl)-3-azabicyclo[3.1.0]hexane → 3-Acetyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Acetyl-1-(p-aminophenyl)-3-azabicyclo[3.1.0]hexane | HCID 20468332 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 3-Acetyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane | HCID 20352243 | — |
Reaction Steps
A solution of 3-acetyl-1-(p-aminophenyl)-3-azabicyclo[3.1.0]hexane in 8N hydrochloric acid is diazotized at 0° C, with aqueous sodium nitrite. The solution is then allowed to stand at ambient temperature until the evolution of nitrogen ceases. This mixture is then extracted with ether, and the extract is dried over sodium sulfate, filtered and then evaporated under reduced pressure to give 3-acetyl-1-(p-hydroxyphenyl)-3-azabicyclo[3.1.0]hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04088652 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-70693089ac8046d4a43e434b407e55c4 |
| Source note | uspto-grants-1978_05 |