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Ammonium Chloride → HCID 86597424、化合物

HRID 1698380
ノート
印刷プレビュー

反応式

HRID 1698380 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 25517Ammonium ChlorideHCID 74580DichloromethoxymethylsilaneHCID 178418314HCID 178418314、化合物

生成物 1

HCID 86597424HCID 86597424、化合物収率 80%

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-bb1d2fc91bca474481316282c1c3a2b2
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08163950B2

反応ノート

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