HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528561Generated: November 3, 2026
Azobisisobutyronitrile → HCID 86712493, compound
https://huagongshe.com/reaction/1528561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 86712494 | HCID 86712494 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 86712493 | HCID 86712493 | — |
Reaction Steps
A mixture of 2-(2,5-bis(hexyloxy)-4-(4-methylbenzo[d]oxazol-2-yl)phenyl)-5-(tert-butyl)benzo[d]oxazol (3.7 g, 6.35 mmol), N-bromosuccinimide (NBS) (1.13 g, 6.35 mmol), and AIBN (0.1 g, 0.6 mmol) in CCl4 (40 mL) was heated to reflux for 15 h under dry argon atmosphere. The reaction mixture was cooled to 0° C. and the precipitate was removed by filtration while maintaining the temperature at 0° C. After the solvent was evaporated, 4-(bromomethyl)-2-(4-(5-(tert-butyl)benzo[d]oxazol-2-yl)-2,5-bis(hexyloxy)phenyl)benzo[d]oxazole was obtained as an oil, which was used for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090602B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-3fb6720d529941a9a54bb7b80a96e9f9 |
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| Source note | uspto-grants-2015_07 |
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