Potassium Persulfate → HCID 70391162、化合物
反応式
[CH3:1][O:2][C:3]([C@H:5]1[N:8](CC2C=CC(OC)=CC=2OC)[C:7](=[O:20])[C@H:6]1[NH:21][C:22](=[O:30])[CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:4].S(OOS([O-])(=O)=O)([O-])(=O)=O.[K+].[K+].P(O)([O-])([O-])=O.[K+].[K+]>C(#N)C.O>[CH3:1][O:2][C:3]([C@H:5]1[NH:8][C:7](=[O:20])[C@H:6]1[NH:21][C:22](=[O:30])[CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:4]参加物
実験手順
A mixture of 412 mg of cis-1-(2,4-dimethoxybenzyl)-3-phenylacetamido-2-oxoazetidine-4-carboxylic acid methyl ester, 810 mg of potassium persulfate and 261 mg of dipotassium phosphate in 20 ml of acetonitrile and 20 ml of water is heated under reflux for one hour. The reaction mixture is concentrated in vacuo and the residue is dissolved in ethyl acetate, and washed successively with an aqueous 5% sodium hydrogen carbonate solution and an aqueous sodium chloride solution, and dried over magnesium sulfate, and the solvent is then distilled off in vacuo. Ethyl acetate is added to the residue and the precipitated crystals are collected by filtration to give cis-3-phenylacetamido-2-oxoazetidine-4-carboxylic acid methyl ester, m.p. 176°-180° C.
後処理
- temperatureis heated
- temperatureunder reflux for one hour
- concentrationThe reaction mixture is concentrated in vacuo
- dissolutionthe residue is dissolved in ethyl acetate
- washwashed successively with an aqueous 5% sodium hydrogen carbonate solution
- dry with materialan aqueous sodium chloride solution, and dried over magnesium sulfate
- distillationthe solvent is then distilled off in vacuo
- additionEthyl acetate is added to the residue
- filtrationthe precipitated crystals are collected by filtration
出典と根拠
- ORDレコード
- ord-491e16f0de6148c68df414a10147bcd0
- 出典データセット
- uspto-grants-1989_04
- 特許番号
- US04822790
反応ノート
読み込み中…