Chlorotrimethylsilane → [(Cyclooct-1-en-1-yl)oxy](trimethyl)silane

HRID 542633ノート

反応式

HRID 542633 の反応式
Cl[Si:2]([CH3:5])([CH3:4])[CH3:3].C(N(CC)CC)C.[C:13]1(=[O:21])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.CCCCCC>CN(C)C=O>[C:13]1([O:21][Si:2]([CH3:5])([CH3:4])[CH3:3])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH:14]=1

参加物

6

実験手順

To a solution of 42 g (0.38 mol) of chlorotrimethylsilane and 78 g of triethylamine in 100 ml of dimethylformamide, a solution of 32 g (0.254 mol) of cyclooctanone in 40 ml of dimethylformamide was added. The resultant mixture was stirred at 100° to 115° C. for 48 hours. At the end of the reaction, the reaction mixture was combined with 240 ml of n-hexane and washed twice with 300 ml of a saturated aqueous sodium bicarbonate solution. The mixture was washed under cooling with 180 ml of 1.5N hydrochloric acid, then washed sequentially with an aqueous sodium bicarbonate solution, water, and saline and then dried with magnesium sulfate. The mixture was concentrated and distilled under a vacuum, to afford 40 g (80% in yield) of 1-cyclooctenyloxytrimethylsilane having a boiling point of 82° to 84° C./5 mmHg.

後処理

  1. customAt the end of the reaction
  2. washwashed twice with 300 ml of a saturated aqueous sodium bicarbonate solution
  3. washThe mixture was washed
  4. temperatureunder cooling with 180 ml of 1.5N hydrochloric acid
  5. washwashed sequentially with an aqueous sodium bicarbonate solution, water, and saline
  6. dry with materialdried with magnesium sulfate
  7. concentrationThe mixture was concentrated
  8. distillationdistilled under a vacuum

出典と根拠

ORDレコード
ord-097d42ba0f35440086fea782c76a27ad
出典データセット
uspto-grants-1987_04
特許番号
US04658055

反応ノート

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