Ethyl chloroformate → o-Ethoxycarbonylbenzamidoxime
反応式
[C:1](Cl)(=[O:5])[O:2][CH2:3][CH3:4].Cl.[C:8](=[N:16][OH:17])([NH2:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>C(Cl)(Cl)Cl>[CH2:3]([O:2][C:1]([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[C:8](=[N:16][OH:17])[NH2:15])=[O:5])[CH3:4]参加物
実験手順
Following the known process [Ber, 18, 2467 (1875)], a solution of 13.4 ml (0.14 mol) of ethyl chlorocarbonate in 100 ml of chloroform was added dropwise to a solution of 38.2 g (0.28 mol) of benzamidoxime hydrochloride in 380 ml of chloroform. After completion of the dropwise addition, the reaction mixture was stirred at room temperature for 3 hours. The benzamidoxime thus precipitated was filtered off and the filtrate was concentrated under reduced pressure. The residue was dissolved in 100 ml of ethyl alcohol, to which 30 ml, of water were added. Most ethyl alcohol was then distilled off under reduced pressure. Crystals thus formed were collected by filtration, washed with water and then dried under reduced pressure, whereby the title compound was obtained as colorless crystals.
後処理
- additionAfter completion of the dropwise addition
- customThe benzamidoxime thus precipitated
- filtrationwas filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- dissolutionThe residue was dissolved in 100 ml of ethyl alcohol, to which 30 ml, of water
- additionwere added
- distillationMost ethyl alcohol was then distilled off under reduced pressure
- customCrystals thus formed
- filtrationwere collected by filtration
- washwashed with water
- dry with materialdried under reduced pressure, whereby the title compound
- customwas obtained as colorless crystals
出典と根拠
- ORDレコード
- ord-3da0b65f184c44a0b41acf88ef98320d
- 出典データセット
- uspto-grants-1992_05
- 特許番号
- US05112841
反応ノート
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