HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-acetamido-2,3-dimethyl-N-(p-tolylsulfonyl)butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2,4-Dimethyl-4-isopropyl-2-oxazolin-5-one | HCID 14695765 | — |
| Reactant | Sodium p-toluene sulfonamide | HCID 66664522 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-acetamido-2,3-dimethyl-N-(p-tolylsulfonyl)butyramide | HCID 14624688 | — |
Reaction Steps
2,4-Dimethyl-4-isopropyl-2-oxazolin-5-one (2.0 g) is mixed with DMF (50 mL), THF (70 mL) and sodium p-toluene sulfonamide (5.0 g), and the resulting mixture is heated at reflux for 16 hours. At the end of this time the mixture is cooled, and the solvents are removed under vacuum. The residue is mixed with water and the pH adjusted to 8 with NaHCO3. The aqueous mixture is extracted with ethyl acetate and the organic layers are discarded. The aqueous mixture is acidified to pH~4 with HCl and saturated with NaCl and extracted with ethyl acetate. The organic extracts are combined, dried over MgSO4, filtered and evaporated to give 0.66 of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05120854 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-5af8b1bdae29495e975b54f0d6658438 |
| Source note | uspto-grants-1992_06 |