Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,5-Dimethylanisole | HCID 74350 | — |
| Reactant | 2,5-Bis(bromomethyl)benzonitrile | HCID 23250090 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 22908569 | HCID 22908569 | — |
Reaction Steps
These monomers are commercially available or can be prepared by a simple modification. A very suitable monomer is α,α'-dibromo-2-cyano-p-xylene (see formula V of FIG. 2), which can be prepared by refluxing a mixture of 2,5-dimethylbenzonitryl, N-bromosuccinimide and benzoyl peroxide in carbon tetrachloride for several hours. The solid formed is recrystallized from a mixture of petroleum ether and toluene and subsequently dried under a vacuum. Another suitable monomer is α,α'-dibromo-2-methoxy-p-xylene (see formula VI of FIG. 2), which can be prepared by refluxing a mixture of 2,5-dimethylanisol, N-bromosuccinimide and benzoyl peroxide in carbon tetrachloride in a nitrogen atmosphere for several hours. The solid formed is recrystallized from hexane and subsequently dried under a vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05670212 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-963bfecfd29c4f0289563bd72e93225e |
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| Source note | uspto-grants-1997_09 |
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