Ammonium Chloride → HCID 86597424, compound

HRID 2373718Notes

Reaction equation

HRID 2373718 reaction equation
[CH:1]([Mg]Cl)([CH2:3][CH3:4])[CH3:2].[CH3:7][Si:8]([O:11][CH3:12])(Cl)Cl.[Cl-].[NH4+]>>[CH:1]([Si:8]([CH:1]([CH2:3][CH3:4])[CH3:2])([CH3:7])[O:11][CH3:12])([CH2:3][CH3:4])[CH3:2]

Participants

4

Procedure

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%).

Workup

  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

Sources & evidence

ORD record
ord-e7de7a5b741f46e08332dc9718222247
Source dataset
uspto-grants-2008_12
Patent number
US07459577B2

Reaction notes

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