反応式
[ClH:1].[C:2]([CH:4]1[C:16]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[C:10]2[C:5]1=[CH:6][CH:7]=[CH:8][CH:9]=2)#[N:3].[CH2:17]([OH:19])[CH3:18]>CCOCC>[CH2:17]([O:19][C:2]([CH:4]1[C:16]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[C:10]2[C:5]1=[CH:6][CH:7]=[CH:8][CH:9]=2)=[NH:3])[CH3:18].[OH2:19].[ClH:1].[ClH:1]参加物
6
実験手順
Dry hydrogen chloride was passed for 3 hours into a solution of 9-cyanofluorene (15 67.85; g.; see, for example, J. Amer. Chem. Soc., 1949, 71, 1500) in ether (1 l.) ans absolute ethanol (45 ml.) at 0°C. The mixture was left at 0°C overnight, the solid filtered, washed with ether and dried under vacuum at room temperature to give the title compound as its hydrochloride hemihydrate (17.61 g., m.p. 262°-263°C dec.). Found: C, 68.5; H, 6.05; N, 4.95%. C16H13NO.HCl.1/2H2O requires C, 687.85; H, 6.05; N, 4.95%.
後処理
- customat 0°C
- filtrationthe solid filtered
- washwashed with ether
- customdried under vacuum at room temperature
出典と根拠
- ORDレコード
- ord-0a5d8286d7bc4bd49403ed3a138078c5
- 出典データセット
- uspto-grants-1976_07
- 特許番号
- US03971782
関連ノート
読み込み中…