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4-(Methylsulfonyl)-3-(trifluoromethyl)benzonitrile → [4-Methanesulfonyl-3-(trifluoromethyl)phenyl]methanamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-(Methylsulfonyl)-3-(trifluoromethyl)benzonitrile | HCID 45933716 | — |
| 触媒 | Nickel | HCID 935 | — |
| 溶媒 | Ammonia | HCID 222 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | [4-Methanesulfonyl-3-(trifluoromethyl)phenyl]methanamine | HCID 66632608 | — |
反応手順
A mixture of 4-fluoro-3-trifluoromethylbenzonitrile (75 mg, 0.40 mmol), sodium sulfinate (44.5 mg, 0.44 mmol) in N,N-dimethylformamide (1.5 mL) was heated at 100° C. for 2 h. The reaction mixture was cooled to room temperature, quenched with water. The resulting white solid was collected via filtration, washed with cold water, dried in a vacuum oven to give 4-methanesulfonyl-3-trifluoromethyl-benzonitrile (90 mg, 90% yield). This benzonitrile was hydrogenated in 2N NH3 in methanol with 35 mg of Raney Ni under a hydrogen balloon for 2 h. The reaction mixture was filtered through a celite plug, washed with methanol, evaporated in vacuo to give the titled compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07888374B2 |
| 出典データセット | uspto-grants-2011_02 |
| ORD ID | ord-f6a0f34fb0a64f62a97a309ec3886341 |
| 出典メモ | uspto-grants-2011_02 |