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2-Chloro-4-fluoro-5-nitrobenzyl cyanide → 2-(5-Amino-2-chloro-4-fluorophenyl)acetonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Chloro-4-fluoro-5-nitrobenzyl cyanide | HCID 23036745 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Nickel | HCID 935 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(5-Amino-2-chloro-4-fluorophenyl)acetonitrile | HCID 23036747 | — |
反応手順
Hydrogen is injected at 25°-30° C., under normal pressure, into a mixture consisting of 8.9 g of 2-chloro-4-fluoro-5-nitrobenzyl cyanide, 1 g of Raney nickel in 90 ml of absolute ethanol, until the stoichiometric amount of hydrogen has been absorbed. After completion of the absorption of hydrogen, the reaction mixture is filtered and the alkaline filtrate is concentrated by evaporation. The residue consists of 7.5 g of 5-amino-2-chloro-4-fluorobenzyl cyanide having a melting point of 85°-86° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04950777 |
| 出典データセット | uspto-grants-1990_08 |
| ORD ID | ord-bcfdc784943f4c81ac6b0e8dd9478f94 |
| 出典メモ | uspto-grants-1990_08 |