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Trichlorosilane → 3-(2-Phenoxyethoxy)propyltrichlorosilane

HRID 129585
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HRID 129585 반응식
[C:1]1([O:7][CH2:8][CH2:9][O:10][CH2:11][CH:12]=[CH2:13])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:14][SiH:15]([Cl:17])[Cl:16]>[H+].[H+].Cl[Pt-2](Cl)(Cl)(Cl)(Cl)Cl>[O:7]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][CH2:13][Si:15]([Cl:17])([Cl:16])[Cl:14])[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

4

반응물 2

HCID 24811TrichlorosilaneHCID 19372171Benzene, [2-(2-propenyloxy)ethoxy]-

생성물 1

HCID 193721673-(2-Phenoxyethoxy)propyltrichlorosilane수율 79.7%

시약·촉매·용매 1

HCID 61859Chloroplatinic acid촉매

반응 조건

온도
70 °C

실험 절차

Under a nitrogen atmosphere, 8 mg of hexachloroplatinic acid are added to 178 g (1.0 mol) of 2-allyloxyethyl phenyl ether, the preparation of which is described above under a), and the mixture is heated to 70° C. 169 g (1.25 mol) of trichlorosilane are added dropwise to the mixture over a period of 2 hours and the mixture is stirred for a further 2 hours at 70° C. The crude product is purified by distillation in vacuo, giving 250 g of 3-(2-phenoxyethoxy)propyltrichlorosilane having an acid number of 531.

후처리

  1. customthe preparation of which
  2. distillationThe crude product is purified by distillation in vacuo

출처 및 근거

ORD 기록
ord-f04507110b894eb7af7f030877207730
출처 데이터셋
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05468890

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