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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618316Generated: October 30, 2026

Potassium Carbonate → 4-Hydroxy-7-phenoxy-1-vinyl-isoquinoline-3-carboxylic acid butyl ester

https://huagongshe.com/reaction/1618316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,4,6-Trivinylboroxin-Pyridine ComplexHCID 2734806—
ReactantButyl 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylateHCID 86595463—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product4-Hydroxy-7-phenoxy-1-vinyl-isoquinoline-3-carboxylic acid butyl esterHCID 66713281—

Reaction Steps

A mixture of 1-Bromo-4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid butyl ester (416 mg, 1 mmol, see example D-28a), Pd(PPh3)4 (118 mg, 0.1 mmol), 2,4,6-Trivinylcyclotriboroxane-pyridine complex (241 mg, 1 mmol), K2CO3 (414 mg, 3 mmol), and 1,4-dioxane (8 ml) was refluxed with stirring under N2 protection for 3 h. Subsequently, the mixture was concentrated in vacuo. To the residue was added water (5 ml) and the mixture was extracted with EtOAc (20 ml). The organic phase was dried over MgSO4 and evaporated in vacuo. Purification of the residue by flash column chromatography on silica gel using hexanes EtOAc=98 2 as the eluent gave the title compound as a yellowish solid (65 mg); MS-(+)-ion M+1=364.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765956B2
Source datasetuspto-grants-2014_07
ORD IDord-6f2a66d73ea64009a78a3edf6b47ab2d
Source noteuspto-grants-2014_07