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Styrene → Phenethyldimethylchlorosilane

HRID 2268187
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HRID 2268187 반응식
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH3:9][SiH:10]([CH3:12])[Cl:11]>[Pt].C1(C)C=CC=CC=1>[CH2:1]([Si:10]([CH3:12])([CH3:9])[Cl:11])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
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참가 물질

5

반응물 2

HCID 7501Styrene3회HCID 66108Chlorodimethylsilane2회

생성물 1

HCID 86970Phenethyldimethylchlorosilane수율 8.4%

시약·촉매·용매 2

HCID 23939Platinum촉매HCID 1140Toluene용매

실험 절차

Reaction between styrene and dimethylchlorosilane with platinum catalyst in the presence of trimethylsilyl-N,N-dimethyl carbamate. 526 mg Styrene and 480 mg dimethylchlorosilane were introduced into a glass tube, and 41 mg of trimethylsilyl-N,N-dimethyl carbamate were added using a microsyringe. 0.65 mg Of a toluene solution of a 0-valent platinum complex of divinylsiloxane (0.4 wt % platinum content) was added. The tube was sealed with Teflon tape and a rubber septum and placed in a 100° C. oil bath where it was heated for 20 hours. After cooling, the tube contents were analyzed by gas chromatography revealing a styrene conversion of 38% and a phenethyl dimethylchlorosilane yield of 8.4%. The ratio between the phenethyl dimethylchlorosilane and the (α-methylbenzene) dimethylchlorosilane was 44:1.

후처리

  1. customplaced in a 100° C.
  2. temperaturewas heated for 20 hours
  3. temperatureAfter cooling

출처 및 근거

ORD 기록
ord-0c3c09b3a7a24d7bb547d0bc91fb84eb
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06326506B1

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