HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792509Generated: November 2, 2026
Azobisisobutyronitrile → HCID 22031053, compound
https://huagongshe.com/reaction/1792509
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | Methyl 4-bromo-2-methylbenzoate | HCID 22031226 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22031053 | HCID 22031053 | 34.2% |
Reaction Steps
A mixture of 458 mg methyl 4-bromo-2-methylbenzoate, 427 mg N-bromosuccinimide, 25 mg α,α′-azobisisobutyronitrile and 10 mL carbon tetrachloride was heated for 30 minutes under reflux. 50 mg N-bromosuccinimide was added thereto, and the mixture was further heated for 30 minutes under reflux. The reaction solution was cooled, insolubles were filtered off, and the filtrate was evaporated. 773 mg crude product of methyl 4-bromo-2-bromomethyl benzoate was obtained as a pale yellow oil. A mixture of this compound, 546 mg 4-fluorobenzyl amine, 0.34 mL triethylamine and 10 mL methanol was heated for 2 days under reflux. The reaction solution was cooled, and the precipitated crystals were collected by filtration and dried under reduced pressure with a vacuum pump, to give 219 mg of the title compound as pale brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07074801B1 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-505d1b14e7004be6bcec09611ab16457 |
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| Source note | uspto-grants-2006_07 |
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