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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481377Generated: October 26, 2026

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

https://huagongshe.com/reaction/481377

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-l-(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 numberUS05789413
Source datasetuspto-grants-1998_08
ORD IDord-6197c4ee24984d6da99e2e74b559676a
Source noteuspto-grants-1998_08