1,3-Dichloropropane → 1,3-Bis(trichlorosilyl)propane
반응식
[Cl:1][CH2:2][CH2:3][CH2:4]Cl.[Cl:6][SiH:7]([Cl:9])[Cl:8]>[Cl-].C([P+](CCCC)(CCCC)CCCC)CCC>[Cl:6][Si:7]([Cl:9])([Cl:8])[CH2:2][CH2:3][CH2:4][Si:7]([Cl:9])([Cl:8])[Cl:6].[Cl:1][CH2:2][CH2:3][CH2:4][Si:7]([Cl:9])([Cl:8])[Cl:6]참가 물질
5
실험 절차
In the same apparatus and procedure as Example 1 above, 0.44 g (1.50 mmol) of tetrabutylphosphonium chloride, 0.85 g (7.5 mmol) of 1,3-dichloropropane, and 10.16 g (75.0 mmol) of trichlorosilane were reacted at 150° C. for 10 hrs. The resulting mixture was distilled to give 1.68 g of 1,3-bis(trichlorosilyl)propane (yield; 72%) and 0.22 g of (3-chloropropyl)trichlorosilane (yield; 14%).
후처리
- distillationThe resulting mixture was distilled
출처 및 근거
- ORD 기록
- ord-4e600918000f4c37a1bb05bb1f3d518f
- 출처 데이터셋
- uspto-grants-2002_05
- 특허 번호
- US06392077B1
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