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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 842695Erstellt: 24. Oktober 2026

Ethanol → Ethyl 6-bromonicotinate

https://huagongshe.com/de/reaction/842695

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
Edukt2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
Edukt6-Bromonicotinic acidHCID 238932—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 6-bromonicotinateHCID 1478466883%

Reaktionsschritte

A mixture of 2-bromopyridine-5-carboxylic acid (J.Org.Chem., 12, 456 (1947)) (2.32 g, 11.49 mmol) and N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (3.12 g, 12.64 mmol) in dichloromethane (30 ml) was stired at room temperature for 1 hour under nitrogen. Absolute ethanol (5 ml) was added and the mixture stirred for 30 minutes and then concentrated under reduced pressure. The residue was partitioned between dichloromethane (40 ml) and 10% w/w aqueous potassium carbonate solution (40 ml). The aqueous layer was extracted with dichloromethane (25 ml) and the combined organic layers were dried (MgSO4) and concentrated under reduced pressure. Purification by flash chromatography on silica gel, eluting with dichloromethane gave 2-bromopyridine-5-carboxylic acid ethyl ester (2.18 g, 83%) as a colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06376490B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-2d91dec768aa4e6bb696860f466d54d7
Quellennotizuspto-grants-2002_04