HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Azide → 4-(2-Naphthoyl)-3,5-dichlorobenzyl azide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 4-(2-Naphthoyl)-3,5-dichlorobenzyl bromide | HCID 14700027 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2-Naphthoyl)-3,5-dichlorobenzyl azide | HCID 14700028 | 103.6% |
Reaction Steps
A suspension of 4-(2-naphthoyl)-3,5-dichlorobenzyl bromide (0.633 g, 1.61 mmol) and sodium azide (0.245 g, 3.77 mmol) in 10 ml of ethanol was heated at reflux for 3 hours. The reaction mixture was filtered and the precipitate rinsed with ethanol. The filtrate was concentrated and the residue redissolved in ether. The resulting precipitate was collected and washed thoroughly with ether. Concentration afforded 0.594 g of an oil which slowly crystallized. The crude azide was used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04923885 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-65223d951e464d58a32c339488d46a80 |
| Source note | uspto-grants-1990_05 |