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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1162583Erstellt: 25. Oktober 2026

N-bromobutanimide → Ethyl 6-(bromomethyl)picolinate

https://huagongshe.com/reaction/1162583

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
EduktEthyl 6-methylpyridine-2-carboxylateHCID 564597—
KatalysatorBenzoyl PeroxideHCID 7187—
LösungsmittelCarbon TetrachlorideHCID 5943—
ProduktEthyl 6-(bromomethyl)picolinateHCID 2303375598,3%

Reaktionsschritte

A mixture of 6-methyl-pyridine-2-carboxylic acid ethyl ester (1.65 g, 10 mmol), NBS (1.77 g, 10 mmol), and benzoyl peroxide (100 mg) in carbon tetrachloride (20 ml) was refluxed for 14 h. After cooling to room temperature, the reaction mixture was partitioned between diethyl ether and water (120 ml, 4:1), organic layer was washed with water (2×20 ml), brine, dried (MgSO4), filtered and concentrated to give 6-bromomethyl-pyridine-2-carboxylic acid ethyl ester (2.4 g) which was used without further purification. LCMS m/z: 245 (M+1)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07820704B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-68468710087740078ac5874558b61ab5
Quellennotizuspto-grants-2010_10