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Triethylamine → N-(4-nitrobenzyl)trifluoroacetoamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2,2,2-Trifluoroethyl Acetate | HCID 136256 | — |
| 反応物 | 4-Nitrobenzylamine hydrochloride | HCID 11252467 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-(4-nitrobenzyl)trifluoroacetoamide | HCID 14317262 | — |
反応手順
To a suspension of 4-nitrobenzylamine hydrochloride (10.0 g) and triethylamine (22.2 ml) in acetonitrile (100 ml) was added trifluoroethyl acetate (12.6 ml) at room temperature and the mixture was stirred for 24 hours. The solvent was removed under reduced pressure, water was added to the mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure. The precipitated crystals were collected by filtration. The crystals were washed with hexane, to give N-(4-nitrobenzyl)trifluoroacetoamide (12.79 g) as colorless crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07262185B2 |
| 出典データセット | uspto-grants-2007_08 |
| ORD ID | ord-2b75692cde864675be581d7fbd123640 |
| 出典メモ | uspto-grants-2007_08 |