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Formaldehyde → 2-Cyano-2-(4-chlorophenyl)propan-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Benzyltriethylammonium hydroxide | HCID 74601 | — |
| 反応物 | 2-(4-Chlorophenyl)propiononitrile | HCID 102762 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-Cyano-2-(4-chlorophenyl)propan-1-ol | HCID 14032851 | — |
反応手順
To an ice cold stirred solution of α-methyl-4-chlorobenzyl cyanide* (50 g., 0.3 mole) in 500 ml. of pyridine containing a suspension of paraformaldehyde (36 g., 1.2 mole) is added 1 ml. of benzyl triethylammonium hydroxide. The mixture is stirred under nitrogen at room temperature for 72 hours. The reaction mixture is poured into water and extracted with ether. The combined ether extracts are washed with water, saturated sodium chloride solution and dried over magnesium sulfate. The solvent is evaporated to give a thick oil, 58.4 g, which is identified by nmr.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04225723 |
| 出典データセット | uspto-grants-1980_09 |
| ORD ID | ord-9c9ff106b56b47b58e0e163f8e96d101 |
| 出典メモ | uspto-grants-1980_09 |