Toluene → n-Butanephosphonic acid n-butyl-(3-nitrophenyl) ester
反応式
[Cl-].[CH2:2]([O:6][P:7]([CH2:10][CH2:11][CH2:12][CH3:13])(=[O:9])[OH:8])[CH2:3][CH2:4][CH3:5].[N+:14]([C:17]1C=C([O-])[CH:20]=[CH:21][CH:22]=1)([O-:16])=[O:15].[Na+].[C:25]1(C)C=CC=C[CH:26]=1>>[CH2:4]([C:3]1[C:17]([N+:14]([O-:16])=[O:15])=[CH:22][CH:21]=[CH:20][C:2]=1[O:6][P:7]([CH2:10][CH2:11][CH2:12][CH3:13])(=[O:8])[OH:9])[CH2:5][CH2:25][CH3:26]参加物
4
実験手順
20 g of n-butanephosphonic acid n-butyl ester chloride are added dropwise to a suspension of 14.3 g of sodium 3-nitrophenolate in 170 ml toluene at 20° C. After 4 hours, the mixture is filtered, the filtrate is evaporated and the residue is distilled in vacuo at 0.1 mm Hg. 16 g of n-butanephosphonic acid n-butyl-(3-nitrophenyl) ester are obtained. After reduction with hydrogen and palladium on charcoal, in isopropanol, at 1 atmosphere pressure, 13.8 g of n-butanephosphonic acid n-butyl-(3-aminophenyl) ester are obtained.
後処理
- filtrationthe mixture is filtered
- customthe filtrate is evaporated
- distillationthe residue is distilled in vacuo at 0.1 mm Hg
出典と根拠
- ORDレコード
- ord-42fd0b9be195461284cfc75024ca34b2
- 出典データセット
- uspto-grants-1977_05
- 特許番号
- US04026709
反応ノート
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