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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523841Generated: October 31, 2026

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

https://huagongshe.com/reaction/523841

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 numberUS09339527B2
Source datasetuspto-grants-2016_05
ORD IDord-a89d6d0071734502963ca4cf1393b49f
Source noteuspto-grants-2016_05