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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634350Generated: November 1, 2026

Cesium carbonate → 3-(1-Hydroxyethyl)-4-phenyl-1H-isochromen-1-one

https://huagongshe.com/reaction/634350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Bromo-3-(1-hydroxyethyl)-1H-isochromen-1-oneHCID 118131255—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-(1-Hydroxyethyl)-4-phenyl-1H-isochromen-1-oneHCID 118131164—

Reaction Conditions

Temperature120 °C

Reaction Steps

4-Bromo-3-(1-hydroxyethyl)-1H-isochromen-1-one (Intermediate A2, 0.77 g, 2.88 mmol), phenylboronic acid (0.63 g, 5.18 mmol), Pd(PPh3)4 (0.199 g, 0.173 mmol) and Cs2CO3 (1.49 g, 4.6 mmol) were dissolved in DMF (10.7 ml) and heated under microwave irradiation at 120° C. for 20 min. The reaction mixture was then diluted with AcOEt (100 mL) and filtrate. The organic phase was washed twice with 0.5 M HClaqueous, twice with water, sat NaHCO3 and once with sat NaClaqueous. The resulting organic phase was dried over Na2SO4, filtered and concentrated. The crude was finally purified on Biotage Si 50 g Ultra with a gradient of Hexane and EtOAc. The title compound was recovered as dark pink solid (0.53 g, 1.99 mmol, 69.3%) as a dark pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321776B2
Source datasetuspto-grants-2016_04
ORD IDord-5fb022e6d905482a98a2d3bc662e3ad6
Source noteuspto-grants-2016_04