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Water → t-Butyl N-(2-benzoylphenyl)-N-(p-toluenesulfonyl)aminoacetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | tert-Butyl bromoacetate | HCID 79177 | — |
| 反応物 | N-(2-Benzoylphenyl)-4-methylbenzenesulfonamide | HCID 233206 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | t-Butyl N-(2-benzoylphenyl)-N-(p-toluenesulfonyl)aminoacetate | HCID 18688807 | 95.4% |
反応手順
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%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | USRE036832 |
| 出典データセット | uspto-grants-2000_08 |
| ORD ID | ord-aa24dcc414ce4a0db5e75eb596a02395 |
| 出典メモ | uspto-grants-2000_08 |