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Triethylamine → 2-Butyramido-4-nitrophenyl trifluoromethanesulfonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| 反応物 | N-(2-hydroxy-5-nitrophenyl)butanamide | HCID 3599768 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Butyramido-4-nitrophenyl trifluoromethanesulfonate | HCID 11291234 | — |
反応手順
To a solution of N-(2-hydroxy-5-nitrophenyl)butyramide (Compound 117, 1.75 g, 7.8 mmol) in CH2Cl2 (40 ml) at 0° C. was added Et3N (1.4 ml, 10.1 mmol) and Tf2O (1.7 ml, 10.2 mmol). After 10 min, the reaction was diluted with CH2Cl2, washed with H2O and brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→25% EtOAc-hexanes) to yield the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524917B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-da175815e55247df81ca8bc698266e3a |
| 出典メモ | uspto-grants-2013_09 |