HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 18386111, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 18385579 | HCID 18385579 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18386111 | HCID 18386111 | — |
Reaction Steps
50 mg of 2,2-dimethyl-5-{4-(methylsulfonyl)phenyl}-4-{4-(methylthio)-phenyl}-3(2H)-furanone (Example 72) in 10 ml dichloromethane and 2 ml methanol was stirred with 300 mg of OXONE at room temperature for 4 hours. The insoluble material was filtered off and the filtrate was washed with aqueous sodium bicarbonate. The organic layer was then concentrated under reduced pressure and was purified by column chromatography (ethylacetate) to give 45 mg of 2,2-dimethyl-4,5-di{4-(methylsulfonyl)phenyl}-3(2H)-furanone. mp: 245-257° C. NMR: δ1.60 (s, 6H), 3.08 (s, 3H), 3.10 (s, 3H), 7.50-7.53 (m, 2H), 7.79-7.82 (m, 2H), 7.94-8.00 (m, 4H). IR (cm−1): 2931, 1698, 1510, 1387, 1258, 1150, 960, 846, 770.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492416B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-e3658c78d6b9493cbb67a9725d362990 |
| Source note | uspto-grants-2002_12 |