反応式
C(OC([N:8]([CH2:19][CH2:20][CH2:21][P:22](=[O:33])([O:28]CCCC)[O:23]CCCC)[O:9]CC1C=CC(OC)=CC=1)=O)C(C)C.Cl>C(O)(=O)C>[OH:9][NH:8][CH2:19][CH2:20][CH2:21][P:22](=[O:23])([OH:33])[OH:28]参加物
4
実験手順
A mixture of dibutyl 3-[N-isobutoxycarbonyl-N-(p-methoxybenzyloxy)amino]propylphosphonate (6.04 g), conc. hydrochloric acid (60 ml) and acetic acid (60 ml) was refluxed with stirring for 21 hours. The resultant mixture was concentrated under reduced pressure, and to the residue was added water. The mixture was concentrated under reduced pressure to give a residue, which was washed with acetonitrile and then dissolved in water (10 ml). To the solution were added pyridine (800 ml) and ethanol (4 ml), and then the mixture was allowed to stand overnight at 4° C. to give 3-(N-hydroxyamino)propylphosphonic acid (1.02 g) in the form of crystals. MP: 160°-166° C. (dec.).
後処理
- temperaturewas refluxed
- concentrationThe resultant mixture was concentrated under reduced pressure
- additionto the residue was added water
- concentrationThe mixture was concentrated under reduced pressure
- customto give a residue, which
- washwas washed with acetonitrile
- dissolutiondissolved in water (10 ml)
- additionTo the solution were added pyridine (800 ml) and ethanol (4 ml)
- waitto stand overnight at 4° C.
出典と根拠
- ORDレコード
- ord-d8cddff232904b7992445f9a2bfc898e
- 出典データセット
- uspto-grants-1980_06
- 特許番号
- US04206156
関連ノート
読み込み中…