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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862581Generated: November 1, 2026

Azobisisobutyronitrile → HCID 54529045, compound

https://huagongshe.com/reaction/862581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
ReactantPhthalimide potassium saltHCID 24194345—
ReactantHCID 54156513HCID 54156513—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 54529045HCID 5452904556.3%

Reaction Steps

A mixture of diethyl 3-methyl-6-nitrobenzylmalonate (25.0 g, 80.8 mmol), N-bromosuccinimide (18.5 g, 103.9 mmol), and azobisisobutyronitrile (AlBN, 1.1 g) in carbon tetrachloride (400 mL) was refluxed for 11 h, while 3×100 mg of AlBN were added every 3 h during the reaction. The insoluble material formed was removed by filtration and the filtrate was concentrated. The residue was dissolved in DMF (100 mL) and potassium phthalimide (13.5 g, 72.9 mmol) was added. The mixture was stirred for 3 h at 5°~60° C., poured into saturated sodium bicarbonate, and extracted with a 1:1 mixture of toluene and ethyl acetate. The organic layers were washed with brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography with 4:1 hexane/ethyl acetate to give 18.66 g of the title compound (51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719152
Source datasetuspto-grants-1998_02
ORD IDord-d9c6abd3fb784c6696a2508ad879057e
Source noteuspto-grants-1998_02