2-(4-Phenoxyphenoxy)ethyl ethylcarbamate → N-ethyl-N-2-(4-phenoxyphenoxy)ethoxycarbonyl-oxamic acid ethyl ester
反応式
[O:1]([C:8]1[CH:22]=[CH:21][C:11]([O:12][CH2:13][CH2:14][O:15][C:16](=[O:20])[NH:17][CH2:18][CH3:19])=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl-].[CH2:24]([O:26][C:27](=[O:31])[C:28]([OH:30])=O)[CH3:25]>C(Cl)CCl>[CH2:24]([O:26][C:27](=[O:31])[C:28]([N:17]([CH2:18][CH3:19])[C:16]([O:15][CH2:14][CH2:13][O:12][C:11]1[CH:21]=[CH:22][C:8]([O:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:9][CH:10]=1)=[O:20])=[O:30])[CH3:25]参加物
4
実験手順
9.0 g of N-ethyl-carbamic acid-2-(4-phenoxyphenoxy)ethyl ester are dissolved in 90 ml of ethylene chloride. To this solution are added 9.6 g of oxalic acid monoethyl ester chloride, and stirring is maintained for 10 hours under mild refluxing conditions. The cooled reaction mixture is then poured into 200 ml of ice-water, and the organic phase is separated. This is washed with cold water, dried over sodium sulfate, concentrated by evaporation and taken up in dichloromethane. Chromatography on silica gel with dichloromethane as the eluant thus yields the compound of the formula ##STR6## in the form of white crystals having a m.p. of 56°-58° C.
後処理
- temperatureis maintained for 10 hours
- temperatureunder mild refluxing conditions
- customThe cooled reaction mixture
- customthe organic phase is separated
- washThis is washed with cold water
- dry with materialdried over sodium sulfate
- concentrationconcentrated by evaporation
- customChromatography on silica gel with dichloromethane as the eluant thus yields the compound of the formula ##STR6## in the form of white crystals
出典と根拠
- ORDレコード
- ord-dbb256ec12ac46e6a675f898862614f3
- 出典データセット
- uspto-grants-1985_11
- 特許番号
- US04554290
反応ノート
読み込み中…