HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium azide → 3,5-Dichloro-4-(4-chlorobenzoyl)benzyl azide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium azide | HCID 10290740 | — |
| Reactant | 4-(4-Chlorobenzoyl)-3,5-dichlorobenzyl bromide | HCID 13649656 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,5-Dichloro-4-(4-chlorobenzoyl)benzyl azide | HCID 13649662 | 100.9% |
Reaction Steps
A suspension of 4-(4-chlorobenzoyl)-3,5-dichlorobenzyl bromide (3.2 g, 8.5 mmol) and potassium azide (1.3 g, 16 mmol) in ethanol (32 ml) was refluxed 5 hours, cooled, and filtered. The precipitate was washed once with ethanol and the combined filtrate and wash were evaporated under vacuum. The residue was triturated with diethyl ether (50 ml) and filtered. The filtrate was evaporated under vacuum to provide 2.92 g (100%) of 4-(4-chlorobenzoyl)-3,5-dichlorobenzyl azide, m.p. 50°-55° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04590201 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-d349e108594544a898b47cc88d46c300 |
| Source note | uspto-grants-1986_05 |