HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Azide → 1-[4-(2-Azidoethyl)phenyl]ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 1-(4-(2-Bromoethyl)phenyl)ethan-1-one | HCID 611194 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-[4-(2-Azidoethyl)phenyl]ethan-1-one | HCID 19809185 | — |
Reaction Steps
p-(2-Bromoethyl)-acetophenone (J.A.C.S. 62, 1940, 1435) was reacted with sodium azide in dimethyl sulphoxide to give p-(2-azidoethyl)acetophenone. Oxidation with sodium hypobromide gave p-(2-azidoethyl)benzoic acid (melting point 130°-131°, from acetone/hexane) which was converted with thionyl chloride into the corresponding acid chloride. Treatment of the acid chloride with ammonia gave p-(2-azidoethyl)benzamide. Treatment with triphenylphosphine and hydrolysis gave p-(2-aminoethyl)benzamide of melting point 132°-133° (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04585796 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-7a23315d1cc842c9a59c83b7f9092ac8 |
| Source note | uspto-grants-1986_04 |