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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523804Generated: October 25, 2026

Sodium Carbonate → 4-Benzyloxy-1-p-tolyl-isoquinoline-3-carboxylic acid butyl ester

https://huagongshe.com/reaction/523804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTolylboronic acidHCID 79799—
Reactant4-Benzyloxy-1-bromo-isoquinoline-3-carboxylic acid butyl esterHCID 86014503—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyloxy-1-p-tolyl-isoquinoline-3-carboxylic acid butyl esterHCID 66712754105.8%

Reaction Steps

4-Benzyloxy-1-bromo-isoquinoline-3-carboxylic acid butyl ester (207 mg, 0.5 mmol) and Pd(PPh3)4 (23 mg, 0.02 mmol) were dissolved in THF (3 ml) and the solution was stirred for 10 min before a solution of p-tolylboronic acid (68 mg, 0.5 mmol) in EtOH (0.5 ml) and a solution of Na2CO3 (106 mg, 1 mmol) in water (0.5 ml) were added. The resulting mixture was refluxed with stirring for 4 h. Subsequently, the mixture was concentrated in vacuo. To the residue was added water (2 ml) and the mixture was extracted with EtOAc (10 ml). The organic phase was dried over MgSO4 and evaporated in vacuo to give a yellowish oil (225 mg). Purification by flash column chromatography on silica gel using hexanes:EtOAc=94:6 as the eluent gave the title compound as a colorless oil; MS-(+)-ion: M+1=426.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339527B2
Source datasetuspto-grants-2016_05
ORD IDord-bba576c62d7a4dc395acfedfc93b7e70
Source noteuspto-grants-2016_05