Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339037Generated: October 25, 2026

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

https://huagongshe.com/reaction/339037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-Methyl dicyclohexylamineHCID 24210—
ReactantEthyl trans-crotonateHCID 429065—
Reactant8-Bromo-2-methylquinolineHCID 4715030—
CatalystHCID 178418851HCID 178418851—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product(Z)-ethyl 3-(2-methylquinolin-8-yl)but-2-enoateHCID 7098352935.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-95ffce153e0a46418ceb309f184b570f
Source noteuspto-grants-2014_11