HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 1-Methoxy-3-(methylsulfonyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 3-Methoxythioanisole | HCID 281182 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Methoxy-3-(methylsulfonyl)benzene | HCID 259650 | 98% |
Reaction Steps
To a solution of 3-methoxythioanisole (3.084 g, 20 mmol) in 300 mL acetone was added a solution of oxone (30.74 g, 50 mmol) in 125 mL water, resulting in the formation of a white precipitate. Stirring continued overnight, and the solid was filtered off and washed with acetone. Filtrate was concentrated to remove acetone. Aqueous layer was extracted with EtOAc (2×200 mL) and dried over Na2SO4. The solvent was removed to give 1-methanesulfonyl-3-methoxy benzene (3.68 g, 98%) as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242144B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-a77d81cc485c4568ba517ff9cedff5b1 |
| Source note | uspto-grants-2012_08 |