Carbon Dioxide → 2-(4-Chlorobenzyl)-1-methylperhydroazepine
反応式
C(OC([C:6](=[C:14]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][N:15]1[CH3:21])[C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=1)=O)C.C(=O)=O.[OH-].[Na+]>Cl>[Cl:13][C:10]1[CH:11]=[CH:12][C:7]([CH2:6][CH:14]2[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][N:15]2[CH3:21])=[CH:8][CH:9]=1参加物
実験手順
Boil 15.5 g of 2-(α-ethoxycarbonyl-4-chlorobenzylidene)- 1-methylperhydroazepine and 110 ml of concentrated hydrochloric acid under reflux until the evolution of CO2 ceases. Cool the resulting reaction mixture to ambient temperature; then alkalize it with caustic soda solution (while cooling with ice) and extract the product with diethyl ether. Concentrate the ether phase and dry the prepared concentrate over sodium sulfate. Dissolve the residual 2-(4-chlorobenzylidene)-1-methylperhydroazepine (7.44 g) in ethyl alcohol and hydrogenate with platinum/active carbon/hydrogen. Filter the catalyst from the hydrogenated product, distil off the solvent and then distil the remainder under a high vacuum to obtain 4.4 g of the title compound with a BP of 102° to 110° at 0.003 mm of Hg.
後処理
- temperatureCool
- customthe resulting reaction mixture to ambient temperature
- extractionextract the product with diethyl ether
- concentrationConcentrate the ether phase
- customdry the prepared
- concentrationconcentrate over sodium sulfate
- dissolutionDissolve the residual 2-(4-chlorobenzylidene)-1-methylperhydroazepine (7.44 g) in ethyl alcohol
- filtrationFilter the catalyst from the hydrogenated product
- customdistil off the solvent
- customdistil the remainder under a high vacuum
出典と根拠
- ORDレコード
- ord-9cb96ea3457a47809df237889174aaf9
- 出典データセット
- uspto-grants-1980_09
- 特許番号
- US04221788
反応ノート
読み込み中…