反応式
[C:1]([O-:4])(=[O:3])[CH3:2].[K+].Cl[CH2:7][SiH2:8][CH:9]([O:12][CH3:13])[O:10][CH3:11]>[Br-].C([P+](CCCC)(CCCC)CCCC)CCC.C(OCCOCCOCCCC)CCC>[C:1]([O:4][CH2:7][SiH2:8][CH:9]([O:12][CH3:13])[O:10][CH3:11])(=[O:3])[CH3:2]参加物
実験手順
Example 2 was repeated using potassium acetate (405 g, 4.13 mol) and (chloromethyl)dimethoxymethylsilane (535 g, 3.46 mol) as starting materials, tetrabutylphosphonium bromide (35.0 g, 10.3 mmol) as catalyst and diethylene glycol dibutyl ether (525 mL) as solvent. After the reaction, the product was distilled at 10 mbar (head), 61-70° C. (head) and 80-119° C. (pot) through a packed column (20 cm) to obtain 560 g (3.14 mol, 91% of theory) of (acetoxymethyl)-dimethoxymethylsilane in the distillate; purity 98.0% (GC area %). The solvent then started to pass over at 10 mbar (head), 118° C. (head) and 124° C. (pot); by distilling over about 10 g of solvent, the (acetoxymethyl)dimethoxymethylsilane was fully removed from the residue. The solvent, potassium chloride, excess potassium acetate and the phase transfer catalyst (in the form of the bromide, chloride and acetate salt of tetrabutylphosphonium) remained in the residue.
後処理
- customAfter the reaction
- distillationthe product was distilled at 10 mbar (head), 61-70° C. (head) and 80-119° C. (pot) through a packed column (20 cm)
出典と根拠
- ORDレコード
- ord-1ae6698a9fea467c960df6ac1a9893dd
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08692012B2
関連ノート
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