HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazolone → 2-acetamido-2,3-dimethyl-N-(p-tolylsulfonyl)butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazolone | HCID 504 | — |
| Reactant | 4-Isopropyl-2,4-dimethyl-1-(p-tolylsulfonyl)-2-imidazolin-5-one | HCID 14624660 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-acetamido-2,3-dimethyl-N-(p-tolylsulfonyl)butyramide | HCID 14624688 | — |
Reaction Steps
The reaction mixture is checked for completeness of formation of 4-isopropyl-2,4-dimethyl-1-(p-tolylsulfonyl)-2-imidazolin-5-one by infrared spectroscopy. The product imidazolin-5-one is then hydrolyzed by diluting the solution with 100 mL of methylene cloride and washing twice with water and once with HCl 10%. The organic layer is concentrated in vacuo and the resulting yellowish oily residue is shaken with ether and allowed to stand. Upon standing the title product precipitates as a white solid, which after filtration, washing and drying has a mp of 202°-203° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05338883 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-836dcabbd3604ebb8eb2bfdeaa885b55 |
| Source note | uspto-grants-1994_08 |