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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441156Generated: October 26, 2026

Sulfuric Acid → 3-(4-(Methylthio)phenyl)-2-phenylinden-1-one

https://huagongshe.com/reaction/441156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantHexaneHCID 8058—
Reactant4-BromothioanisoleHCID 66037—
ReactantBenzylidenephthalideHCID 68464—
ReactantSodium BicarbonateHCID 516892—
ReactantButyllithiumHCID 178418339—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-(4-(Methylthio)phenyl)-2-phenylinden-1-oneHCID 15337399—

Reaction Steps

To a solution of p-bromothioanisole (2.04 g, 10 mmol) in THF (40 mL) cooled to -78° C. was added a solution of n-butyl lithium in hexane (4.0 mL of 2.5M, 10 mmol). The resulting suspension was stirred at this temperature for 20 min. Then a solution of benzalphthalide (2.11 g, 9.5 mmol) in benzene (20 mL) was added and the reaction was allowed to proceed at r.t. for 2 hrs. The reaction turned deep-red. The reaction was completed by addition of conc. H2SO4 (0.63 mL, 20 mmol) and stirred at r.t. for another 30 min. The reaction was then diluted with EtOAc and a 1:1 mixture of H2O and saturated aqueous NaHCO3 and extracted. The aqueous layer was extracted one more time with EtOAc. The combined organic extracts were dried over MgSO4 and concentrated to dryness. The crude product was purified by flash chromatography eluted with 10-15% EtOAc in hexane to give the title compound as an orange-red gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521213
Source datasetuspto-grants-1996_05
ORD IDord-eec2145e21774616acd9a6fbb3f09b9e
Source noteuspto-grants-1996_05