[C:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH:10]1[CH:14]([CH2:15][N+:16]([O-:18])=[O:17])[CH2:13][CH2:12][C:11]1=[O:19])([OH:3])=[O:2].[C:20]1([CH3:30])C=CC(S(O)(=O)=O)=CC=1.[OH2:31]>C1C=CC=CC=1.C(O)CO>[CH2:30]1[CH2:20][O:31][C:10]2([CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][C:1]([OH:3])=[O:2])[CH:14]([CH2:15][N+:16]([O-:18])=[O:17])[CH2:13][CH2:12][CH:11]2[O:19]1The solution of 2-(6-carboxyhexyl)-3-nitromethyl-cyclopentan-1-one, methyl ester (14 g.) in benzene (200 ml.), ethylene glycol (16.1 ml.), p-toluenesulphonic acid (0.315 g.), is heated to boiling for 16 hours. The reaction water is separated in a Marcusson apparatus. The mixture is washed with an aqueous saturated NaHCO3 -solution (50 ml.), then with water to neutrality, dried over sodium sulphate and the solvent is evaporated in vacuo. From the oily residue, by chromatography on silica (300 g.) and elution with benzene/ethyl acetate (6:1), 13 g. of 1-ethylenedioxy-2-(6-carboxyhexyl)-3-nitromethyl-cyclopentane, methyl ester, are obtained.
読み込み中…
