HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(4-(Methanesulfonyl)phenyl)-2-phenylinden-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Monoperoxyphthalic Acid Magnesium Salt | HCID 10130449 | — |
| Reactant | HCID 15337399 | HCID 15337399 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(4-(Methanesulfonyl)phenyl)-2-phenylinden-1-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521213 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-412b7d6753d94ec6b6ce90b88f8f6fd9 |
| Source note | uspto-grants-1996_05 |