HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078084Generated: November 1, 2026
Azobisisobutyronitrile → HCID 15672392, compound
https://huagongshe.com/reaction/1078084
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,3-Pyridinedicarboxylic acid, 5-methyl-, 2,3-dimethyl ester | HCID 11745869 | — |
| Reactant | HCID 15672391 | HCID 15672391 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 15672392 | HCID 15672392 | 57% |
Reaction Steps
A mixture of dimethyl 5-methyl-2,3-pyridinedicarboxylate (30.0 g, 0.143 mol), N-bromosuccinimide (32.0 g, 0.18 mol) and 2,2'-azobisisobutyronitrile (0.9 g, 0.0055 mol) in carbon tetrachloride (200 mL) is heated at 80° C. for 1.5 hours. Additional 2,2'-azobisisobutyronitrile (0.9 g, 0.0055 mol) is added and the reaction mixture is heated at reflux for 2 hours, cooled to room temperature and filtered. The filter cake is washed with carbon tetrachloride. The filtrate and wash are combined, washed with water and concentrated in vacuo to give an oil. The oil is shown by HPLC to contain 57% of the title product, 16% dimethyl 5-methyl-2,3-pyridinedicarboxylate and 23% dimethyl 5-dibromomethyl-2,3-pyridinedicarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05545835 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-2c40abd583c94340885c2e4fe10ad240 |
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| Source note | uspto-grants-1996_08 |
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