Iodine → Diisopropyl(3-methoxypropyl)silane

HRID 1169568ノート

反応式

HRID 1169568 の反応式
Br[CH2:2][CH2:3][CH2:4][O:5][CH3:6].[Mg].II.[CH:10]([SiH:13]([CH:15]([CH3:17])[CH3:16])Cl)([CH3:12])[CH3:11].[Cl-].[NH4+]>C1COCC1>[CH:10]([SiH:13]([CH:15]([CH3:17])[CH3:16])[CH2:2][CH2:3][CH2:4][O:5][CH3:6])([CH3:12])[CH3:11]

参加物

7

反応条件

温度
55 °C

実験手順

1-Bromo-3-methoxypropane (9.18 g, 60.0 mmol) was dissolved in THF (55 mL), and magnesium (1.53 g, 62.9 mmol) and iodine (catalytic amount) were added thereto, followed by stirring at room temperature for 20 minutes and at 55° C. for 5 minutes. The resultant mixture was added dropwise to diisopropylchlorosilane (8.88 mL, 52.0 mmol) in THF (65 mL) for 5 minutes, followed by stirring at room temperature for 1 hour. After termination of exothermic reaction, the resultant mixture was further stirred at 50° C. for 1.5 hours, and saturated aqueous ammonium chloride was added thereto. The resultant mixture was extracted with pentane, followed by washing with water six times and drying over sodium sulfate anhydrate. The solvent was removed under reduced pressure, whereby the Compound 60a was obtained as an yellow liquid (10.1 g, 89%).

後処理

  1. stirringby stirring at room temperature for 1 hour
  2. customAfter termination of exothermic reaction
  3. extractionThe resultant mixture was extracted with pentane
  4. washby washing with water six times
  5. dry with materialdrying over sodium sulfate anhydrate
  6. customThe solvent was removed under reduced pressure, whereby the Compound 60a

出典と根拠

ORDレコード
ord-5bd981af22ff45e48334337ac71934da
出典データセット
uspto-grants-2010_11
特許番号
US07825103B2

反応ノート

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