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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298265Generated: October 29, 2026

Sodium Carbonate → 2,2-dimethyl-5-(4-(methylsulfonyl)phenyl)-4-p-tolylfuran-3(2H)-one

https://huagongshe.com/reaction/2298265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantTolylboronic acidHCID 79799—
Reactant4-Bromo-2,2-dimethyl-5-[4-(methylsulfonyl)phenyl]-3(2h)-furanoneHCID 18385727—
CatalystHCID 178418397HCID 178418397—
CatalystHCID 178420549HCID 178420549—
SolventBenzeneHCID 241—
Product2,2-dimethyl-5-(4-(methylsulfonyl)phenyl)-4-p-tolylfuran-3(2H)-oneHCID 1838573766.9%

Reaction Steps

To a stirred solution of 4-bromo-2,2-dimethyl-5-{4-(methylsulfonyl)phenyl}-3(2H)-furanone (110 mg) and tetrakis(triphenylpalladium(0) (54 mg) in 30 ml benzene, were added 2 M aqueous sodium carbonate (0.22 ml) and 4-methyl-benzeneboronic acid (60 mg). The reaction solution was stirred at reflux for 24 hours. Then the solvent was evaporated off under reduced pressure. The resulting residue was extracted with 50 ml water and dichloromethane (50 ml×3). The organic layer was concentrated in vacuo and the resulting residue was separated by column chromatography (hexane/ethylacetate=2:1) to give 76 mg of 2,2-dimethyl-4-(4-methylphenyl)-5-{4-(methylsulfonyl)phenyl}-3(2H)-furanone as a solid. mp: 167-168° C. NMR: δ1.57 (s, 6H), 2.38 (s, 3H), 3.07 (s, 3H), 7.17 (m, 4H), 7.89 (m, 4H). IR (cm−1): 1707, 1660, 1531, 1289, 1230. MS (EI): 356 (m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492416B1
Source datasetuspto-grants-2002_12
ORD IDord-ed5d0f6d2149453abc2e45f05bd1a4fb
Source noteuspto-grants-2002_12