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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099983Generated: November 1, 2026

Azobisisobutyronitrile → 6-Bromomethyl-nicotinic acid methyl ester

https://huagongshe.com/reaction/2099983

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-methyl nicotinate (1.05 g, 10 mmol) was dissolved in ethyl acetate (50 ml), followed by addition of NBS (3.56 g, 20 mmol) and AIBN (329 mg, 2 mmol). After stirring at 80° C. for 3 hours, aqueous sodium bicarbonate was added and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane; 4/1) to give the title compound (682 mg, 28%) as orange amorphous product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569570B2
Source datasetuspto-grants-2009_08
ORD IDord-d2681e5412e5407d821cd0f72119893a
Source noteuspto-grants-2009_08