Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 215829Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3-(6-Methoxy-pyridin-3-yloxy)-benzoic acid ethyl ester

https://huagongshe.com/de/reaction/215829

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
EduktEthyl 3-hydroxybenzoateHCID 24522—
Edukt5-Bromo-2-methoxypyridineHCID 2734895—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelPyridineHCID 1049—
Produkt3-(6-Methoxy-pyridin-3-yloxy)-benzoic acid ethyl esterHCID 6729714423,6%

Reaktionsschritte

A suspension of 5-bromo-2-methoxy-pyridine (5.4 g, 29 mmol), ethyl 3-hydroxybenzoate (4.0 g, 24 mmol), K2CO3 (4.3 g, 30 mmol), Cu powder (0.30 g, 4.8 mmol) and CuI (0.30 g, 1.56 mmol) in pyridine (25 ml) was refluxed for 18 h. The resulting mixture was mixed with 100 g of crushed ice, neutralized with 1N hydrochloric acid to pH 7.5 and extracted with ether. The extract was evaporated in vacuo, the obtained crude product was purified by column chromatography on silica (eluent hexanes-ethyl acetate 8:1) to afford 1.55 g (20%) of 3-(6-methoxy-pyridin-3-yloxy)-benzoic acid ethyl ester as colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193192B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-44adbd6a96364be3b0f83d8ea7a0810e
Quellennotizuspto-grants-2012_06