Dichlorodimethylsilane → Chloro(4-ethoxyphenyl)dimethylsilane

HRID 247658

反応式

HRID 247658 の反応式
[Mg].[CH2:2]([O:4][C:5]1[CH:10]=[CH:9][C:8](Br)=[CH:7][CH:6]=1)[CH3:3].[Cl:12][Si:13](Cl)([CH3:15])[CH3:14]>O1CCCC1>[Cl:12][Si:13]([C:8]1[CH:9]=[CH:10][C:5]([O:4][CH2:2][CH3:3])=[CH:6][CH:7]=1)([CH3:15])[CH3:14]

参加物

5

実験手順

To a stirred suspension of 3.5 g (0.14 mole) of magnesium powder in 100 ml of dry tetrahydrofuran was added dropwise 17.5 g (0.14 mole) of p-bromophenyl ethyl ether during a one hour period. The mixture was warmed for one hour and then cooled to room temperature. The reaction mixture was added dropwise to a solution of dichlorodimethylsilane in 100 ml of dry tetrahydrofuran which was cooled to -78° C. Upon completion of addition the reaction mixture was allowed to warm to room temperature. Stirring was continued overnight. After dilution with hexane, the reaction mixture was filtered through celite, and the solvent was evaporated under reduced pressure, leaving a liquid residue. Distillation of this residue yielded 18 g of chloro(4-ethoxyphenyl)dimethylsilane as a clear, colorless oil, b.p. 79°-81° C./0.09 mm of Hg.

後処理

  1. temperatureThe mixture was warmed for one hour
  2. temperaturewas cooled to -78° C
  3. additionUpon completion of addition the reaction mixture
  4. temperatureto warm to room temperature
  5. filtrationAfter dilution with hexane, the reaction mixture was filtered through celite
  6. customthe solvent was evaporated under reduced pressure
  7. customleaving a liquid residue
  8. distillationDistillation of this residue

出典と根拠

ORDレコード
ord-3447a11bccb34c50a85ae6c2c3bc3cdb
出典データセット
uspto-grants-1987_11
特許番号
US04709068

関連ノート

読み込み中…