HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-Bromo-1-(bromomethyl)-2-iodobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Bromo-2-iodo-1-methylbenzene | HCID 15442947 | — |
| Catalyst | Benzyl Peroxide | HCID 11229634 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 4-Bromo-1-(bromomethyl)-2-iodobenzene | HCID 53231307 | 24.2% |
Reaction Steps
N-Bromosuccinimide (NBS) (1.1 molar equivalents, 66.5 g, 373 mmol) and benzyl peroxide (0.006 molar equivalent, 450.7 mg, 1.9 mmol) are added to a solution of 2-iodo-4-bromotoluene 6 (1 molar equivalent, 100.3 g, 338 mmol) in chlorobenzene (1200 ml). The batch is then stirred under reflux overnight. After the solvent has been removed in a rotary evaporator, ethyl acetate and water are added. The aqueous phase is extracted by shaking with ethyl acetate. The organic phase is washed by shaking with water, dried and evaporated in a rotary evaporator. The product 7 (30.7 g, 24%) is obtained in the form of a white powder by recrystallisation from ethanol (50 ml).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580395B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-c1654333ecc6495ebafb0d1456e354dd |
| Source note | uspto-grants-2013_11 |