HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 4-(Difluoromethoxy)benzyl Bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | alpha,alpha-Difluoro-p-methylanisole | HCID 74104 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(Difluoromethoxy)benzyl Bromide | HCID 2737001 | 62.6% |
Reaction Steps
270 g of 4-difluoromethoxytoluene in 800 ml of CCl4 were initially introduced and 300 g N-bromo-succinimide were added. After adding a pinch of azobisisobutyronitrile, the mixture was heated to the reflux temperature. After 8 hours, it was cooled, the insoluble succinimide was filtered off and the residue on the filter was washed with CCl4. The carbon tetrachloride was distilled off from the reaction solution and the crude product was purified by fractional distillation. 250 g of 4-difluoromethoxy-benzyl bromide were obtained. Boiling point=82°-5° C./0.4 mm Hg; nD20 =1.5200.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04405639 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-9b6ebbc0c3ee42a69c80b52d37d69a4c |
| Source note | uspto-grants-1983_09 |