反应 #1256750

ord-5bd981af22ff45e48334337ac71934da

反应方程式

CC(C)[SiH](Cl)C(C)C
diisopropylchlorosilane
[Mg]
magnesium
II
iodine
[Cl-].[NH4+]
ammonium chloride
COCCCBr
1-Bromo-3-methoxypropane
COCCC[SiH](C(C)C)C(C)C
liquid
收率 103.1%
COCCC[SiH](C(C)C)C(C)C
Diisopropyl(3-methoxypropyl)silane
收率 103.1%

溶剂

反应条件

温度
55°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGby stirring at room temperature for 1 hour
  2. 2
    其他After termination of exothermic reaction
  3. 3
    萃取The resultant mixture was extracted with pentane
  4. 4
    洗涤by washing with water six times
  5. 5
    干燥drying over sodium sulfate anhydrate
  6. 6
    其他The solvent was removed under reduced pressure, whereby the Compound 60a

实验过程

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%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07825103B2uspto-grants-2010_11