HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039089Generated: November 4, 2026
Azobisisobutyronitrile → 2-Methyl-5-nitroisoindolin-1-one
https://huagongshe.com/reaction/1039089
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-methyl-4-nitrobenzoate | HCID 15088700 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Methyl-5-nitroisoindolin-1-one | HCID 59225299 | — |
Reaction Steps
AIBN (84 mg, 0.51), NBS (1.1 gram, 6.4 mmol), and the methyl 2-methyl-4-nitrobenzoate (1 g, 5.1 mmol, as prepared in Step 1, Example 44) were suspended in CCl4 (12.8 ml), the vessel evacuated and backfilled with N2 (2×) and the mixture heated under N2 at 79° C. overnight. The solution was filtered, and concentrated in vacuum. One third of the crude material was dissolved in 2 N methylamine in methanol (18 ml), 2N methylamine in THF added (18 ml) and the solution stirred for 2 hours at RT. The volatiles were removed in vacuum and the product was purified by chromatography on SiO2 eluting with 10% acetone:DCM to give the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552022B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-91ac261f03a248548ab47fb554f4e77d |
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| Source note | uspto-grants-2013_10 |
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