Ammonium Chloride → HCID 86597424, compound

The sec-butyl magnesium chloride as prepared above was added dropwise to the methylmethoxydichlorosilane solution as obtained in Example 7, in the same manner as in Example 3(c), to effect the Grignard reaction. The resulting Grignard reaction solution was post-treated with the saturated aqueous ammonium chloride solution as used in Example 3(c) in a reduced amount of 80 ml, instead of the 120 ml. The organic layer was separated and was subjected to a fractional distillation, thereby to afford 31 g of di-sec-butyl methylmethoxysilane as a fraction boiling at 76° C.-78° C./16 mmHg (yield; 80%).

1. customas obtained in Example 7, in the same manner as in Example 3(c)
2. customthe Grignard reaction
3. customThe resulting Grignard reaction solution
4. customThe organic layer was separated
5. distillationwas subjected to a fractional distillation

ORD record

ord-e403968ca1f141dcbe877a1150f63b1c

Source dataset

uspto-grants-2011_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08008521B2