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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594162Generated: November 3, 2026

Azobisisobutyronitrile → 6-Bromomethyl-nicotinic acid methyl ester

https://huagongshe.com/reaction/1594162

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=¼) to give the title compound (682 mg, 28%) as an orange amorphous compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300935B2
Source datasetuspto-grants-2007_11
ORD IDord-8ad3cf375be643c2b8d2c5cc1ca6bef4
Source noteuspto-grants-2007_11