反应 #1256749

ord-0c6668e90da248d08381a4e386a84555

反应方程式

CC(C)[SiH](CC(C)(C)C)C(C)C
Compound 51a
CC(C)[SiH](CC(C)(C)C)C(C)C
Diisopropyl(2,2-dimethylpropyl)silane
CC(C)(C)OCCCBr
1-bromo-3-(tert-butoxy)propane
CC(C)[SiH](CCCOC(C)(C)C)C(C)C
Compound 59a
CC(C)[SiH](CCCOC(C)(C)C)C(C)C
[3-(tert-Butoxy)propyl]diisopropylsilane

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The procedure of synthesizing Compound 51a was repeated, except that 1-bromo-3-(tert-butoxy)propane (5.40 g, 27.7 mmol) was employed, whereby the Compound 59a was obtained as a brown liquid (3.10 g, 49%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07825103B2uspto-grants-2010_11