Ethyl Acetoacetate → Aluminium tris(ethylacetoacetate)
반응식
[CH3:1][CH:2](CC)[O-].[CH3:6][CH:7](CC)[O-].[CH3:11][CH:12](CC)[O-].[Al+3:16].C([O:19][C:20](=[O:25])[CH2:21][C:22]([CH3:24])=[O:23])C>CCCCCCC>[CH2:1]([CH2:24][C:22](=[O:23])[CH2:21][C:20]([O-:19])=[O:25])[CH3:2].[CH2:6]([CH2:24][C:22](=[O:23])[CH2:21][C:20]([O-:19])=[O:25])[CH3:7].[CH2:11]([CH2:24][C:22](=[O:23])[CH2:21][C:20]([O-:19])=[O:25])[CH3:12].[Al+3:16]참가 물질
4
실험 절차
To a flask containing 50.02 g of a mixture of heptane isomers was added 31.0 g (0.125 mol) of aluminium tris(sec-butoxide). To this was added with stirring, 48.37 g (0.376 mol) of ethylacetoacetate. After stirring the liquor was transferred to a rotary evaporator flask and the volatile sec-butanol and heptanes (78.66 g) were removed under vacuum leaving aluminium tris(ethylacetoacetate) (51.23 g, 0.124 mol).