反応式
[CH:1]1[C:14]2[C:5](=[CH:6][C:7]3[C:12]([C:13]=2[CH:15]=O)=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH:4]=[CH:3][CH:2]=1.[CH:17]1([CH2:22][NH2:23])[CH2:21][CH2:20][CH2:19][CH2:18]1.[BH4-].[Na+].Cl>C(O)C>[CH:17]1([CH2:22][NH:23][CH2:15][C:13]2[C:14]3[C:5]([CH:6]=[C:7]4[C:12]=2[CH:11]=[CH:10][CH:9]=[CH:8]4)=[CH:4][CH:3]=[CH:2][CH:1]=3)[CH2:21][CH2:20][CH2:19][CH2:18]1参加物
実験手順
A mixture of 43.5 g of 9-anthraldehyde, 20.97 g of cyclopentylmethylamine and 150 ml of ethanol is heated under reflux for 1.5 hours. The hot solution of N-cyclopentylmethyl-9-anthracenemethyleneimine so obtained is allowed to cool to 60°, and 8.2 g of sodium borohydride is added in small portions, with stirring, while the temperature is maintained at 55-60°. The mixture is then stirred for another 1.5 hours, concentrated hydrochloric acid (35 ml) is added with cooling, and stirring is continued for 0.5 hour. The mixture is then made basic and extracted with methylene chloride. Removal of the solvent from the dried extracts gives 59.1 g of N-cyclopentylmethyl-9-anthracenemethylamine as an oil; nmr spectrum: τ 1.8-3.1 (m, 9); 5.6 (s, 2), 7.5 (d, 7Hz, 2) and 7.8-9.3 (m, 10).
後処理
- temperatureis heated
- temperatureunder reflux for 1.5 hours
- customThe hot solution of N-cyclopentylmethyl-9-anthracenemethyleneimine so obtained
- temperatureto cool to 60°
- temperatureis maintained at 55-60°
- stirringThe mixture is then stirred for another 1.5 hours
- temperaturewith cooling
- stirringstirring
- extractionextracted with methylene chloride
- customRemoval of the solvent from the dried extracts
出典と根拠
- ORDレコード
- ord-71c9fb391f66432c9d27227f781421bd
- 出典データセット
- uspto-grants-1978_03
- 特許番号
- US04077977
関連ノート
読み込み中…