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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069860Generated: October 30, 2026

Potassium Phosphate, Tribasic → 6-Cyclopropyl-8-fluoro-3,4-dihydroisoquinolin-1(2H)-one

https://huagongshe.com/reaction/2069860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTricyclohexylphosphineHCID 75806—
ReactantCyclopropylboronic acidHCID 2760897—
Reactant6-Bromo-8-fluoro-3,4-dihydroisoquinolin-1(2H)-oneHCID 59473776—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product6-Cyclopropyl-8-fluoro-3,4-dihydroisoquinolin-1(2H)-oneHCID 59473812697.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 6-bromo-8-fluoro-3,4-dihydro-2H-isoquinolin-1-one (1.6 g, 6.5 mmol), tricyclohexylphosphine (0.182 g, 0.65 mmol) and Pd(OAc)2 (0.072 g, 0.032 mmol) in 15 ml toluene placed under argon in a pressure flask was added cyclopropyl boronic acid (1.12 g, 13 mmol), potassium phosphate (6.9 g, 32.5 mmol) and 1.5 ml water. The flask was sealed and the mixture was heated under stirring for 4 hours at 100° C. After cooling the reaction mixture was diluted with ethyl acetate and the organic phase washed with brine, dried with sodium sulfate and concentrated. The residue was purified by flash chromatography (ethyl acetate) affording 0.93 g (71.5% yield) of I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299077B2
Source datasetuspto-grants-2012_10
ORD IDord-ba35b7b5d356428ca7a788f395099874
Source noteuspto-grants-2012_10