Allyl acetate → Tetraethylsilane

HRID 20616

반응식

HRID 20616 반응식
F[B-](F)(F)F.C(OCC=C)(=O)C.C([SiH](CC)CC)C.[CH2:20]([Si:23]([CH2:28][CH3:29])([CH2:26][CH3:27])[CH2:24][CH3:25])[CH:21]=C>C1(C)C=CC=CC=1>[CH2:20]([Si:23]([CH2:28][CH3:29])([CH2:26][CH3:27])[CH2:24][CH3:25])[CH3:21]

참가 물질

6

반응물 4

HCID 11584Allyl acetateHCID 12052TriethylsilaneHCID 26255TetrafluoroborateHCID 11194462Allyltriethylsilane

생성물 1

HCID 12426Tetraethylsilane수율 5%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

In a reactor were placed bis(1,5-cyclooctadiene)iridium tetrafluoroborate [Ir(cod)2]+BF4− (0.05 mmol), allyl acetate (20 mmol), and toluene (3 ml). The mixture was raised in temperature to 80° C. in a nitrogen atmosphere, triethylsilane (Et3SiH)(5 mmol) was added thereto over one hour, and a reaction was conducted at 80° C. for one hour. After the reaction, the reaction mixture was analyzed by gas chromatography to find that allyltriethylsilane was produced in a yield of 54% and tetraethylsilane was by-produced in a yield of 5%.

후처리

  1. customIn a reactor were placed
  2. additionwas added
  3. waita reaction was conducted at 80° C. for one hour
  4. customAfter the reaction
  5. customwas produced in a yield of 54%

출처 및 근거

ORD 기록
ord-49ca4e2f681548ffad2587d89196df70
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07745654B2

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