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4-(4-Nitro-2-(trifluoromethyl)phenylethynyl)pyridine → 4-(2-Pyridin-4-yl-ethyl)-3-(trifluoromethyl)aniline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-(4-Nitro-2-(trifluoromethyl)phenylethynyl)pyridine | HCID 23155274 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | HCID 178418390 | HCID 178418390 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-(2-Pyridin-4-yl-ethyl)-3-(trifluoromethyl)aniline | HCID 23155177 | 85% |
反応手順
In 20 mL of ethanol, 1.3 g (4.45 mmol) of 4-(4-nitro-2-(trifluoromethyl)phenylethynyl)pyridine was dissolved and stirred on 100 mg of 10% palladium carbon overnight at room temperature in a hydrogen atmosphere. The catalyst was removed by filtration and the filtrate was concentrated and the residue was purified by a silica gel column (n-hexane:ethyl acetate=1:2) to obtain 1.0 g (85%) of a target product as a pale yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08609656B2 |
| 出典データセット | uspto-grants-2013_12 |
| ORD ID | ord-22078ad930e2479e9260fca9fb639d29 |
| 出典メモ | uspto-grants-2013_12 |