HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoromethylsulfonamide → HCID 59683172, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoromethylsulfonamide | HCID 79001 | — |
| Reactant | HCID 266341 | HCID 266341 | — |
| Reactant | Magnesium monoxide | HCID 6850729 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Catalyst | Dirhodium tetraacetate | HCID 152122 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59683172 | HCID 59683172 | 91% |
Reaction Steps
2.44 g (10.4 mmol) of 2,2,2-trifluoro-N-(4-methylsulphanylphenyl)acetamide and 2.80 g (18.8 mmol) of trifluoromethylsulphonamide are mixed with 145 ml of dichloromethane. 2.09 g (51.9 mmol) of magnesium oxide, 460 mg (1.04 mmol) of rhodium(II) acetate dimer and 6.68 g (20.75 mmol) of iodobenzene diacetate are added to the mixture. The mixture is stirred at room temperature for 1 hour and then filtered, and the filter cake is washed with dichloromethane. On concentration of the filtrate, crystals separate out and are filtered off with suction and washed with a little dichloromethane. Drying results in 3.60 g (9.42 mmol; yield: 91%) of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943629B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-6e0e543e8ee54d28b79424045cda3610 |
| Source note | uspto-grants-2011_05 |