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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441157Generated: October 25, 2026

Water → 3-(4-(Methanesulfonyl)phenyl)-2-phenylinden-1-one

https://huagongshe.com/reaction/441157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
ReactantMonoperoxyphthalic Acid Magnesium SaltHCID 10130449—
ReactantHCID 15337399HCID 15337399—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-(4-(Methanesulfonyl)phenyl)-2-phenylinden-1-oneHCID 15337396—

Reaction Steps

To an ice cold solution of the compound from Step 1 (525 mg, 1.6 mmol) in CH2Cl2 (16 mL) and MeOH (1.6 mL) was added MMPP (1.09 g, tech. 80%, 1.76 mmol). The resulting suspension was stirred at r.t. for 3 hrs. The reaction was 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 first by flash chromatography, eluted with EtOAc in hexane 35%, and then crystallized from EtOAc/Hexane (1:1, 20 mL) to give the title compound as a bright orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521213
Source datasetuspto-grants-1996_05
ORD IDord-412b7d6753d94ec6b6ce90b88f8f6fd9
Source noteuspto-grants-1996_05