Toluene → n-Butanephosphonic acid n-butyl-(3-nitrophenyl) ester

HRID 1287313ノート

反応式

HRID 1287313 の反応式
[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

反応物 3

HCID 1140TolueneHCID 86734044n-Butanephosphonic acid n-butyl ester chlorideHCID 101286967CID 101286967

生成物 1

HCID 54481294n-Butanephosphonic acid n-butyl-(3-nitrophenyl) ester

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 of 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-nitro-phenyl) 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

  1. filtrationthe mixture is filtered
  2. customthe filtrate is evaporated
  3. distillationthe residue is distilled in vacuo at 0.1 mm Hg

出典と根拠

ORDレコード
ord-b27ad6561a674dbda93a5ed7932fb409
出典データセット
uspto-grants-1976_10
特許番号
US03984432

反応ノート

読み込み中…