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Triphenylphosphine → Silane, trichloro[(trimethylsilyl)methyl]-

HRID 1068514
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반응식

HRID 1068514 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.Cl[CH2:21][Si:22]([CH3:25])([CH3:24])[CH3:23].[Cl:26][SiH:27]([Cl:29])[Cl:28]>>[Cl:26][Si:27]([Cl:29])([Cl:28])[CH2:21][Si:22]([CH3:25])([CH3:24])[CH3:23].[Cl:26][SiH:27]([Cl:28])[CH2:21][Si:22]([CH3:25])([CH3:24])[CH3:23]
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참가 물질

5

반응물 3

HCID 11776TriphenylphosphineHCID 24811TrichlorosilaneHCID 75361Silane, (chloromethyl)trimethyl-

생성물 2

HCID 11816894Silane, trichloro[(trimethylsilyl)methyl]-수율 70%HCID 57370759HCID 57370759, 화합물수율 7%

실험 절차

In the same apparatus and procedure as Example 1 above, 0.20 g (0.75 mmol) of triphenylphosphine, 1.38 g (7.5 mmol) of (chloromethyl)trimethylsilane, and 5.08 g (37.5 mmol) of trichlorosilane were reacted at 150° C. for 10 hrs. The resulting mixture was distilled to give 1.2 g of 1,1,1,-trichloro-3,3-dimethyl-1,3-disilabutane (bp; 173-174° C., yield; 70%) and 0.1 g of 1,1-dichloro-3,3-dimethyl-1,3-disilabutane (bp; 157-159° C., yield; 7%).

후처리

  1. distillationThe resulting mixture was distilled

출처 및 근거

ORD 기록
ord-e4864bfb00c945da96b981a3089537cc
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06251057B1

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