Hydrochloric Acid → 2-(4-(4-Chlorobutanoyl)phenyl)-2-methylpropanoic acid
反応式
[CH:1]1([C:4](=[O:21])[C:5]2[CH:10]=[CH:9][C:8]([C:11]([CH3:20])([CH3:19])[C:12]3[O:13]CC(C)(C)N=3)=[CH:7][CH:6]=2)[CH2:3][CH2:2]1.[ClH:22].[O:23]1CCOCC1>>[Cl:22][CH2:2][CH2:3][CH2:1][C:4]([C:5]1[CH:10]=[CH:9][C:8]([C:11]([CH3:20])([CH3:19])[C:12]([OH:23])=[O:13])=[CH:7][CH:6]=1)=[O:21]参加物
4
実験手順
A mixture of 4-(cyclopropyl-oxo-methyl)-α,α-dimethyl-α-(4,4-dimethyloxazolin-2-yl)toluene, prepared according to Example 3, (42 g, 0.15 mole), 150 mL concentrated hydrochloric acid, and 150 mL 1,4-dioxane was brought to reflux for 18 hours. The mixture was extracted three times with ethyl acetate. The organics were washed with saturated NaCl solution, dried over MgSO4, and concentrated. Crude product was purified by column chromatography using 240 g silica gel, and eluting with 81:14:5 hexanes/ethyl acetate/acetic acid. Cleaner fractions were combined and recrystallized from methylene chloride/hexanes to afford 27 g of 4-(4-chloro-1-oxobutyl)-α,α-dimethylphenylacetic acid as a white solid (68%).