反応式
[OH-].[Na+].[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10](=[N:12][OH:13])[CH3:11])=[CH:6][CH:5]=1.[C:14]([OH:18])(=[O:17])[CH:15]=[CH2:16]>C(O)C.O>[CH3:11][C:10](=[N:12][O:13][CH2:16][CH2:15][C:14]([OH:18])=[O:17])[C:7]1[CH:6]=[CH:5][C:4]([Cl:3])=[CH:9][CH:8]=1参加物
実験手順
A solution of 2.4 g of sodium hydroxide in 55 ml of 85% ethanol was mixed with 6,78 g of 4'-chloroacetophenone oxime and 2.88 g of acrylic acid. The mixture was then refluxed for 2.5 hours, subsequently diluted with 10 ml of water, and concentrated by evaporation in a vacuum after 2 hours. The residue was dissolved in 50 ml of ether and 50 ml of water, and the layers were separated. The water layer was extracted with 50 ml of ether and then acidified with 40 ml of 2 N hydrochloric acid. The acid solution was extracted with 100 ml of ether and the ethereal solution was dried over sodium sulfate. Then the solvent was distilled off and its last traces were removed together with higher boiling substances at a pressure of 0.01 mm and a temperature of 50° C. The residue was crystallized from petroleum ether. Melting point 80° C.-83° C.
後処理
- temperatureThe mixture was then refluxed for 2.5 hours
- concentrationconcentrated by evaporation in a vacuum after 2 hours
- dissolutionThe residue was dissolved in 50 ml of ether
- custom50 ml of water, and the layers were separated
- extractionThe water layer was extracted with 50 ml of ether
- extractionThe acid solution was extracted with 100 ml of ether
- dry with materialthe ethereal solution was dried over sodium sulfate
- distillationThen the solvent was distilled off
- customits last traces were removed together with higher boiling substances at a pressure of 0.01 mm
- customa temperature of 50° C
- customThe residue was crystallized from petroleum ether
出典と根拠
- ORDレコード
- ord-7b876a5a10b94343af915cc4c246854b
- 出典データセット
- uspto-grants-1980_04
- 特許番号
- US04196216
関連ノート
読み込み中…