HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Azido-3-chlorobenzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-Azido-2-chloro-4-methylbenzene | HCID 15433382 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Azido-3-chlorobenzyl bromide | HCID 11482000 | 58% |
Reaction Steps
4-Azido-3-chlorotoluene (17.14 g, 0.1 mol) was dissolved in dry benzene (80 ml) and thereto were added N-bromosuccinimide (19.6 g, 0.11 mol) and AIBN (1.64 g, 0.01 mol). The resulting mixture was refluxed in the shade in a nitrogen stream for 10 hr. Water (100 ml) was added and the mixture was filtrated. The aqueous layer of the filtrate was taken and extracted with ether. The organic layers were combined, washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the obtained brown oil was purified by silica gel column chromatography (eluent; hexane) to give the title compound (14.2 g, yield 58%). m.p.: 75-77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998595 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-4bc15961e8e341c2973c4a48ecfcfe72 |
| Source note | uspto-grants-1999_12 |