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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 339037Erstellt: 24. Oktober 2026

Water → (Z)-ethyl 3-(2-methylquinolin-8-yl)but-2-enoate

https://huagongshe.com/de/reaction/339037

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktN-Methyl dicyclohexylamineHCID 24210—
EduktEthyl trans-crotonateHCID 429065—
Edukt8-Bromo-2-methylquinolineHCID 4715030—
KatalysatorHCID 178418851HCID 178418851—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt(Z)-ethyl 3-(2-methylquinolin-8-yl)but-2-enoateHCID 7098352935,2%

Reaktionsschritte

A solution of 8-bromo-2-methylquinoline (2.00 g, 9.01 mmol), (E)-ethyl but-2-enoate (3.36 mL, 27.0 mmol), N-cyclohexyl-N-methylcyclohexanamine (5.79 mL, 27.0 mmol), and Pd(PtBu3)2 (0.23 g, 0.45 mmol) in dioxane (10 mL) was stirred at reflux for 20 hours. After cooling to ambient temperature, water (20 mL) and ethyl acetate (30 mL) were added. The organic layer was separated, washed with brine, dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue was purified by C-18 reverse phase flash chromatography (Biotage SP4 unit, C-18 40M column, 0-100% CH3CN/water gradient; 30 column volumes) to give (Z)-ethyl 3-(2-methylquinolin-8-yl)but-2-enoate (0.81 g, 35.2%) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889704B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-95ffce153e0a46418ceb309f184b570f
Quellennotizuspto-grants-2014_11