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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529167Generated: October 30, 2026

Azobisisobutyronitrile → 6-Bromomethyl-nicotinic acid methyl ester

https://huagongshe.com/reaction/529167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 6-methylnicotinateHCID 231548—
ReactantSodium BicarbonateHCID 516892—
SolventEthyl AcetateHCID 8857—
Product6-Bromomethyl-nicotinic acid methyl esterHCID 1275223729.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl 6-methylnicotinate (1.05 g, 10 mmol) was dissolved in ethyl acetate (50 ml), and NBS (3.56 g, 20 mmol) and AIBN (329 mg, 2 mmol) were added thereto. The reaction mixture was stirred at 80° C. for 3 hours, combined with an aqueous solution of sodium hydrogen carbonate and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/4) to give the title compound (682 mg, 28%) as an orange amorphous compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346822B2
Source datasetuspto-grants-2016_05
ORD IDord-cd1181c0c009494ab2d03f960a51ef92
Source noteuspto-grants-2016_05