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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486533Generated: October 29, 2026

Sodium Carbonate → HCID 90017824, compound

https://huagongshe.com/reaction/1486533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantToluene ethanolHCID 21863594—
Reactant1-Benzhydryl-5-iodo-pyrimidine-2,4-dioneHCID 71654965—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 90017824HCID 9001782462%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-Benzhydryl-5-iodo-pyrimidine-2,4-dione (0.06 g, 0.15 mmol) was suspended in a 1:1 toluene/ethanol mixture (1,6 Phenylboronic acid (0.03 g, 0.22 mmol) was added followed by 2M aqueous solution of sodium carbonate (0.082 mL, 0.16 mmol). The resulting suspension was degassed under nitrogen atmosphere for 10 min, then tetrakis(triphenylphosphine) palladium(0) (0.017 g, 0.015 mmol) was added. The reaction was heated under microwave irradiation at 100° C. for 30 min. The reaction mixture was diluted with EtOAc and water was added. The two phases were separated and the aqueous layer was extracted with EtOAc (3×15 mL). The combined organic phases were dried over Na2SO4 and the solvent was removed under reduced pressure. The crude was purified by column chromatography using a Teledyne ISCO apparatus (cyclohexane:EtOAc 60:40) to afford the title compound (0.03 g, 62%) as pale yellow solid. 1H NMR (400 MHz, CDCl3): δ 7.13 (s, 1H), 7.20-7.24 (m, 5H), 7.25 (s, 1H), 7.32-7.35 (m, 5H), 7.37-7.44 (m, 5H), 8.19 (br s, 1H). MS (ESI) to/z: 355 [M-H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428465B2
Source datasetuspto-grants-2016_08
ORD IDord-20a472e1d2654df69a3beb3f6f2a7269
Source noteuspto-grants-2016_08