Iodine → n-Hexyl(i-butyl)dichlorosilane

HRID 726829

반응식

HRID 726829 반응식
[Mg].II.[CH2:4](Br)[CH:5]([CH3:7])[CH3:6].[CH2:9]([Si:15](Cl)([Cl:17])[Cl:16])[CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]>C(OCC)C.CCCCCC.O1CCCC1>[CH2:9]([Si:15]([CH2:4][CH:5]([CH3:7])[CH3:6])([Cl:17])[Cl:16])[CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]

참가 물질

8

실험 절차

Anhydrous diethyl ether (125 mL) was put into a reactor with magnesium (5.0 g, 0.21 mol) which had been dehydrated and deaerated, followed by charging of argon gas. A small amount of iodine was slowly added to the mixture. i-Butylbromide (25 g, 0.18 mol) was added dropwise to the slowly stirred mixture so that the reaction mixture was gradually refluxed. After the reaction was complete, the obtained Grignard reagent was transferred to a dropping funnel. The Grignard reagent was added dropwise to a solution being stirred containing n-hexyltrichlorosilane (64 g, 0.25 mol) in anhydrous diethyl ether (50 mL)/anhydrous tetrahydrofuran (50 mL) in another reactor which had been dehydrated and deaerated, followed by charging of argon gas, at 50° C.-60° C. The reaction mixture was then stirred overnight at room temperature. Hexane (500 mL) was added to the reaction mixture, and the resulting mixture was filtered under pressure, followed by fractional distillation of the filtrate to provide the desired product.

후처리

  1. temperaturewas gradually refluxed
  2. customby charging of argon gas, at 50° C.-60° C
  3. stirringThe reaction mixture was then stirred overnight at room temperature
  4. filtrationthe resulting mixture was filtered under pressure
  5. distillationfollowed by fractional distillation of the filtrate

출처 및 근거

ORD 기록
ord-a459fa1b63774a4cb8f64d45bc62df91
출처 데이터셋
uspto-grants-1998_01
특허 번호
US05710301

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