HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium azide → 4-(4-Chlorobenzoyl)-3-chlorobenzyl azide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium azide | HCID 10290740 | — |
| Reactant | 4-(4-Chlorobenzoyl)-3-chlorobenzyl bromide | HCID 13649654 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4-Chlorobenzoyl)-3-chlorobenzyl azide | HCID 13649661 | 106.1% |
Reaction Steps
A stirred suspension of 4-(4-chlorobenzoyl)-3-chlorobenzyl bromide (1.60 g, 4.65 mmol) and potassium azide (0.715 g, 8.81 mmol) in ethanol (15 ml) was refluxed 5 hours, cooled to ambient temperature, and stirred 16 hours. The solids were filtered and washed twice with ethanol. The combined filtrate and washes were evaporated under vacuum, diluted with diethyl ether (40 ml), filtered, and evaporated under vacuum to provide 1.51 g (106% of theory) of 4-(4-chlorobenzoyl)-3-chlorobenzyl azide, m.p. 33°-33.5° C., suitable for subsequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04590201 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-ee83f3216d8e4f2f9e9b60dabba91e4f |
| Source note | uspto-grants-1986_05 |