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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432877Generated: November 1, 2026

Azobisisobutyronitrile → Methyl 5-(bromomethyl)-6-methoxynicotinate

https://huagongshe.com/reaction/1432877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 6-methoxy-5-methylpyridine-3-carboxylateHCID 54292198—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 5-(bromomethyl)-6-methoxynicotinateHCID 5375661254%

Reaction Steps

A solution containing 6-methoxy-5-methyl-nicotinic acid methyl ester (4.00 g, 22.1 mmol), NBS (5.11 g, 28.7 mmol), and AIBN (0.90 g, 5.5 mmol) in CCl4 (100 mL) is warmed to reflux. After 5 h, the reaction mixture is cooled and then concentrated in vacuo. The residue is dissolved in EtOAc (500 mL) and washed successively with aqueous Na2S2O3 (300 mL), water (100 mL), brine then dried over anhydrous Na2SO4, filtered and concentrated. The crude product is purified by silica gel flash column chromatography (hexane/diethyl ether, 9:1) to provide 3.10 g (54%) of the title compound as a white solid. 1H NMR (300 MHz, CDCl3) δ3.90 (s, 3H), 4.07 (s, 3H), 4.46 (s, 2H), 8.19 (d, J=2.2 Hz, 1H), 8.79 (d, J=2.2 Hz, 1H) ppm; MS (EI): m/z 259 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-690a6db5750a4dc49cf7b0dea202de42
Source noteuspto-grants-2009_11