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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060368Generated: November 1, 2026

Potassium Acetate → 1-Chloroisoquinolin-7-ol

https://huagongshe.com/reaction/2060368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant7-Bromo-1-ChloroisoquinolineHCID 6502024—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
SolventSodium BisulfateHCID 516919—
Product1-Chloroisoquinolin-7-olHCID 4683541594.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

7-Bromo-1-chloroisoquinoline (2.0 g, 8.25 mmol), bis(pinacolato)diboron (2.20 g, 8.66 mmol), potassium acetate (2.43 g, 24.7 mmol) and PdCl2(dppf)DCM adduct (0.337 g, 0.412 mmol) were combined under nitrogen in dioxane (40 mL) and heated in an oil bath at 100° C. for 24 h. The reaction mixture was cooled, diluted with EtOAc (100 mL) and washed with 10% aqueous KHSO4. The organic phase was dried over Na2SO4, filtered and concentrated to an oil. The oil was dissolved in acetone (100 mL) and a solution of OXONE (5.07 g, 8.25 mmol) in water (20 mL) added over 2 min. The reaction mixture was stirred for 10 min, diluted with aqueous sodium bisulfate solution and stirred for an additional 20 min. and then concentrated to remove acetone. The resulting mixture was filtered to give the title compound (1.4 g) which was used without further purification. LRMS (M+H)+=180.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278322B2
Source datasetuspto-grants-2012_10
ORD IDord-dcb0f4f451be40969f610fb1e7728413
Source noteuspto-grants-2012_10