Sodium Hydroxide → sodium 2-[4-[[4-[(2Z)-2-(4-cyanophenyl)-2-methoxyiminoethoxy]phenyl]methoxy]phenyl]cyclopropane-1-carboxylate
Reaktionsgleichung
[OH-].[Na+:2].[C:3]([C:5]1[CH:10]=[CH:9][C:8](/[C:11](=[N:34]/[O:35][CH3:36])/[CH2:12][O:13][C:14]2[CH:33]=[CH:32][C:17]([CH2:18][O:19][C:20]3[CH:25]=[CH:24][C:23]([CH:26]4[CH2:28][CH:27]4[C:29]([OH:31])=[O:30])=[CH:22][CH:21]=3)=[CH:16][CH:15]=2)=[CH:7][CH:6]=1)#[N:4]>>[C:3]([C:5]1[CH:10]=[CH:9][C:8](/[C:11](=[N:34]/[O:35][CH3:36])/[CH2:12][O:13][C:14]2[CH:33]=[CH:32][C:17]([CH2:18][O:19][C:20]3[CH:25]=[CH:24][C:23]([CH:26]4[CH2:28][CH:27]4[C:29]([O-:31])=[O:30])=[CH:22][CH:21]=3)=[CH:16][CH:15]=2)=[CH:7][CH:6]=1)#[N:4].[Na+:2]Komponenten
3
Versuchsvorschrift
Compound 51 was synthesized from sodium hydroxide (0.04 g, 0.96 mmol) and 2-{4-[(4-{[(2Z)-2-(4-cyanophenyl)-2-(methoxyimino)ethyl]oxy}benzyl)oxy]phenyl}cyclopropanecarboxylic acid (0.22 g, 0.48 mmol) by following the procedure described in scheme 12 (0.15 g, yield: 72.40%); Purity: 90.60%.