HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 19098812, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 19098816 | HCID 19098816 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 19098812 | HCID 19098812 | 28.6% |
Reaction Steps
To a solution of 19.94 g (0.06 mol) of 4-methyl-benzene-1,2-diol dibenzoate in 350 mL of carbon tetrachloride was added a catalytic amount of 2,2'-azobisisobutyronitrile, followed by 10.68 g (0.06 mol) of N-bromosuccinimide. The reaction mixture was stirred at room temperature for several days and was then filtered. The filtrate was dried over MgSO4, filtered and evaporated to dryness in a rotary evaporator. Purification of the crude material (24.76 g) by HPLC gave 7.05 g of product which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05288871 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-d25ca221be4d4a16ab7ded46f8439474 |
| Source note | uspto-grants-1994_02 |