Triphenylphosphine → Bis(trichlorosilyl)methane

HRID 1068509

반응식

HRID 1068509 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.Cl[CH2:21][Si:22]([Cl:25])([Cl:24])[Cl:23].[Cl:26][SiH:27]([Cl:29])[Cl:28]>>[Cl:23][Si:22]([Cl:25])([Cl:24])[CH2:21][Si:27]([Cl:29])([Cl:28])[Cl:26].[Cl:23][Si:22]([Cl:25])([Cl:24])[CH2:21][SiH:27]([Cl:28])[Cl:26]

참가 물질

5

반응물 3

HCID 11776TriphenylphosphineHCID 15258Trichloro(chloromethyl)silaneHCID 24811Trichlorosilane

생성물 2

HCID 2756737Bis(trichlorosilyl)methane수율 50%HCID 58212176(Dichlorosilylmethyl)trichlorosilane수율 16%

실험 절차

In the same apparatus and procedure as Example 1 above, 0.20 g (0.75 mmol) of triphenylphosphine, 0.92 g (7.5 mmol) of (chloromethyl)trichlorosilane, and 5.08 g (37.5 mmol) of trichlorosilane were reacted at 150° C. for 42 hrs. The resulting mixture was distilled to give 1.1 g of 1,1,1,3,3,3-hexachloro-1,3-disilapropane (bp; 173-174° C., yield; 50%) and 0.3 g of 1,1,1,3,3-pentachloro-1,3-disilapropane (bp; 166-167° C., yield; 16%).

후처리

  1. distillationThe resulting mixture was distilled

출처 및 근거

ORD 기록
ord-9faab18ac8e0432fa3f36b96f922dcd9
출처 데이터셋
uspto-grants-2001_06
특허 번호
US06251057B1

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