HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 12666304, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(2-Azidoethyl)benzamide | HCID 22390689 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12666304 | HCID 12666304 | — |
Reaction Steps
For the preparation of the starting material of Example 10a, p-(2-bromoethyl)-acetophenone was reacted with sodium azide in dimethylsulfoxide to give p-(2-azidoethyl)acetophenone. Oxidation with sodium hypobromite gave p-(2-azidoethyl)benzoic acid (m.p. 130°-131°, from acetone-hexane), which was converted with thionyl chloride into the corresponding acid chloride and subsequently with ammonia into p-(2-azidoethyl)benzamide. Treatment with triphenylphosphine and hydrolysis gave p-(2-aminoethyl)benzamide, m.p. 132°-133° (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05064863 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-2b478726163b4a94904e1a4a22c7aad0 |
| Source note | uspto-grants-1991_11 |