関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Trifluoroacetic anhydride | HCID 9845 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Benzeneethanamine, 4-nitro-, hydrochloride (1:1) | HCID 458983 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2,2,2-Trifluoro-N-[2-(4-nitro-phenyl)-ethyl]-acetamide | HCID 6423744 | — |
反応手順
To a solution of 4-nitrophenethylamine hydrochloride (50 g, 0.247 mole), DIEA (128 mL, 0.74 mole, 3 eq.) and CH2Cl2 (500 mL) in a 1 L round bottom flask equipped with a magnetic stirrer was added (CF3CO)2O (52.5 mL, 0.37 mole, 1.5 eq) dropwise at 5-10° C. (with ice/water bath). After stirring for another 1 h after the addition at RT, the reaction was quenched with water (200 mL) and transferred into a separatory funnel. The organic layer was separated, washed with water and sat. NH4Cl, dried over Na2SO4, filtered, concentrated to give a brown oil. The crude was triturated with water (300 mL), filtered and dried on vacuum overnight to give the desired 2,2,2-trifluoro-N-[2-(4-nitro-phenyl)-ethyl]-acetamide as a yellow solid. This can be used for next step without further purification. An analytical sample was obtained through recrystallization from CH3OH/H2O as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08247430B2 |
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| 出典データセット | uspto-grants-2012_08 |
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| ORD ID | ord-b1f2ea9aff9a4066930400f85f987c56 |
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| 出典メモ | uspto-grants-2012_08 |
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