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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131261Erstellt: 26. Oktober 2026

Azobisisobutyronitrile → 6-Bromomethyl-nicotinic acid methyl ester

https://huagongshe.com/reaction/131261

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
EduktHexaneHCID 8058—
EduktN-bromobutanimideHCID 67184—
EduktMethyl 6-methylnicotinateHCID 231548—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt6-Bromomethyl-nicotinic acid methyl esterHCID 1275223735,5%

Reaktionsschritte

To a solution of methyl 6-methylnicotinate (6.3 g) in carbon tetrachloride (100 mL) is added successively N-bromosuccinimide (8.9 g) and 2,2′-azobisisobutyronitrile (342 mg), and the mixture is refluxed under heating for 6 hours. After cooling to room temperature, to the reaction mixture is added n-hexane (300 mL) and the insoluble materials are removed by filtration. The filtrate is concentrated in vacuo and the resultant crude product is purified by column chromatography on silica gel (Solvent; n-hexane:ethyl acetate=10:1) and stirred in n-hexane to give methyl 6-(bromomethyl)nicotinate (3.4 g, yield; 35%) as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384952B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-88834c4755c14761a72f39e7f625bef1
Quellennotizuspto-grants-2008_06