HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → t-Butyl N-(2-benzoylphenyl)-N-(p-toluenesulfonyl)aminoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | N-(2-Benzoylphenyl)-4-methylbenzenesulfonamide | HCID 233206 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | t-Butyl N-(2-benzoylphenyl)-N-(p-toluenesulfonyl)aminoacetate | HCID 18688807 | 95.4% |
Reaction Steps
To a stirred solution of 5.0 g of compound H in 10 cc of dimethylformamide was added 0.56 g of 63% sodium hydride in 5 cc of dimethylformamide under ice-cooling and the mixture was stirred for 30 minutes. Then, 2.3 cc of t-butyl bromoacetate was added dropwise at the same temperature and stirring was continued for 16 hours. Water was added to the reaction mixture and the desired compound was extracted with ethyl acetate. The extract was washed with water and dried over magnesium sulfate. The solvent was distilled off and the crude product thus obtained was washed with hexane to obtain 6.31 g of compound I. Yield: 95.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05464863 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-dd81fccfed25454b923d657c47302f9c |
| Source note | uspto-grants-1995_11 |