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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940136Generated: October 27, 2026

Triethylamine → 3-Phenylthio-4-(4-(methylsulfonyl)phenyl)-5h-furan-2-one

https://huagongshe.com/reaction/1940136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(Phenylthio)acetic acidHCID 59541—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Bromo-4'-(methylsulfonyl)acetophenoneHCID 735823—
SolventAcetonitrileHCID 6342—
Product3-Phenylthio-4-(4-(methylsulfonyl)phenyl)-5h-furan-2-oneHCID 10269135—

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C., triethylamine (335 μL) was added to a solution of thiophenoxyacetic acid (161 mg) and 2-bromo-1-(4-(methylsulfonyl)phenyl) ethanone (272 mg, WO 9500501, example 9, Step 1) in 5 mL of acetonitrile and the mixture was stirred at 0° C. for 1 h. The reaction mixture was then cooled to -20° C. and DBU (265 μL) was added. The mixture was stirred for 30 min. at -20° C. and was quenched by addition of 1N HCl. The product was extracted with EtOAc, dried over sodium sulfate and partially purified by silica gel chromatography. The impure product was recrystalized from EtOAc/Hexane to afford the title compound as a solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05698584
Source datasetuspto-grants-1997_12
ORD IDord-f785b4e70e7341f5ac7671319de490b1
Source noteuspto-grants-1997_12