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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1176757Erstellt: 26. Oktober 2026

N-bromobutanimide → Methyl 6-(bromomethyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/1176757

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
EduktMethyl 6-methylpyridine-2-carboxylateHCID 73022—
KatalysatorBenzoyl PeroxideHCID 7187—
LösungsmittelCarbon TetrachlorideHCID 5943—
ProduktMethyl 6-(bromomethyl)pyridine-2-carboxylateHCID 2147171420,2%

Reaktionsschritte

6-Bromomethyl-pyridine-2-carboxylic acid methyl ester was prepared according to Wells, G. J. et al. (WO 94/11398): A mixture of 6-methyl-pyridine-2-carboxylic acid methyl ester (6.5 g, 43.0 mmol), benzoyl peroxide (25 mg, 0.1 mmol) and NBS (8.5 g, 47.8 mmol) in carbon tetrachloride (250 mL) was heated at reflux overnight. The reaction mixture was cooled to room temperature, filtered, evaporated, and purified by chromatography on flash silica gel, eluting with 15% ethyl acetate/hexane to give 6-bromomethyl-pyridine-2-carboxylic acid methyl ester (2.0 g, 20%) as a white solid. 1HNMR (CDCl3): δ 8.06 (d, J=8.0 Hz, 1H), 7.87 (dd, J=8.0 Hz, 1H), 7.70 (d, J=8.0 Hz, 1H), 4.65 (s, 2H), 4.02 (s, 3H). MS (APCI+): 231 (45), 235 (42).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07842825B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-d9673c2fb2bc45969f422b986ec8dc57
Quellennotizuspto-grants-2010_11