HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Azide → 3-(4-Chlorobenzoyl)-benzyl azide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 3-(4-Chlorobenzoyl)benzyl bromide | HCID 13649653 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-Chlorobenzoyl)-benzyl azide | HCID 13649660 | 100.1% |
Reaction Steps
A mixture of 3-(4-chlorobenzoyl)benzyl bromide (4.2 g, 13.6 mmol) and sodium azide (1.32 g, 20.3 mmol) in ethanol (40 ml) was refluxed for 5 hours, cooled to ambient temperature, and kept 16 hours. The mixture was filtered and the solids were washed twice with ethanol. The combined filtrate and washes were evaporated to dryness under vacuum and the residue was treated with diethyl ether and filtered. The filtrate was evaporated to dryness under vacuum and dried to provide 3.7 g (100%) of 3-(4-chlorobenzoyl)-benzyl azide, m.p. 43°-45° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04590201 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-797ab928d8754b319797ffa3ce390464 |
| Source note | uspto-grants-1986_05 |