HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861995Generated: October 29, 2026
Azobisisobutyronitrile → HCID 12187011, compound
https://huagongshe.com/reaction/861995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | N-(6-Methylpyridin-2-yl)pivalamide | HCID 3251458 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 12187011 | HCID 12187011 | 47% |
| Product | N-[6-(Bromomethyl)pyridin-2-yl]-2,2-dimethylpropanamide | HCID 14326706 | 33% |
Reaction Steps
Carbontetrachloride (CCl4, 300 mL) and the product of Example 1 (50.6 g, 0.26 mol) were added to a 1 L flask equipped with a N2 inlet The solution was stirred until all solid dissolved. N-bromo-succinimide (NBS, 46.8 g, 0.26 mol) was then added to the reaction flask, followed by 2,2'-azobisisobutyronitrile (AIBN, 0.02 g). The reaction was heated to reflux for 6 h with a 500 watt reflector spot lamp. An additional 0.5 eq (23.4 g) of NBS was added to the reaction, and refluxing was continued for 2 h. After cooling the reaction to room temperature, it was filtered and all solvent was removed under reduced pressure. Flash chromatography (15/85 EtOAc/Hex) provided 31.6 g (47%) of title product and 22.2 g (33%) of the title material of Example 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05716964 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-a13d8f64444b4a6fa60c199ffb654212 |
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| Source note | uspto-grants-1998_02 |
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