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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-methyl-4-nitrobenzoateHCID 15088700—
SolventCarbon TetrachlorideHCID 5943—
Product2-Methyl-5-nitroisoindolin-1-oneHCID 59225299—

Reaction Conditions

Temperature79 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552022B2
Source datasetuspto-grants-2013_10
ORD IDord-91ac261f03a248548ab47fb554f4e77d
Source noteuspto-grants-2013_10