Trichloro(chloromethyl)silane → Bis(trichlorosilyl)methane

HRID 1937077

반응식

HRID 1937077 반응식
[Cl-].C([P+](CCCC)(CCCC)CCCC)C1C=CC=CC=1.Cl[CH2:23][Si:24]([Cl:27])([Cl:26])[Cl:25].[Cl:28][SiH:29]([Cl:31])[Cl:30]>>[Cl:25][Si:24]([Cl:27])([Cl:26])[CH2:23][Si:29]([Cl:31])([Cl:30])[Cl:28]

참가 물질

4

반응물 3

HCID 15258Trichloro(chloromethyl)silaneHCID 24811TrichlorosilaneHCID 200231Benzyltributylphosphonium chloride

생성물 1

HCID 2756737Bis(trichlorosilyl)methane수율 68%

실험 절차

In the same apparatus and procedure as Example 1 above, 0.22 g (0.67 mmol) of benzyltributylphosphonium chloride, 1.23 g (6.69 mmol) of (chloromethyl)trichlorosilane, and 2.71 g (20.0 mmol) of trichlorosilane were reacted at 160° C. for 15 hrs. The resulting mixture was distilled to give 1.13 g of 1,1,1,3,3,3-hexachloro-1,3-disilapropane (yield; 68%).

후처리

  1. distillationThe resulting mixture was distilled

출처 및 근거

ORD 기록
ord-02059802c52946f29da4856f0cad71a8
출처 데이터셋
uspto-grants-2002_05
특허 번호
US06392077B1

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