Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triphenylphosphine → Bis(trichlorosilyl)methane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Trichloro(chloromethyl)silane | HCID 15258 | — |
| 반응물 | Trichlorosilane | HCID 24811 | — |
| 생성물 | Bis(trichlorosilyl)methane | HCID 2756737 | 50% |
| 생성물 | (Dichlorosilylmethyl)trichlorosilane | HCID 58212176 | 16% |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06251057B1 |
| 출처 데이터셋 | uspto-grants-2001_06 |
| ORD ID | ord-9faab18ac8e0432fa3f36b96f922dcd9 |
| 출처 메모 | uspto-grants-2001_06 |