Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzene → 1,2-Bis(o-anisylphenylphosphino) ethane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzene | HCID 241 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Trichlorosilane | HCID 24811 | — |
| 반응물 | 1,2-Bis(o-anisylphenylphosphinyl) ethane | HCID 86734501 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 1,2-Bis(o-anisylphenylphosphino) ethane | HCID 15061558 | — |
반응 단계
Reduction of 1,2-bis(o-anisylphenylphosphinyl) ethane was accomplished by refluxing 16.5 g. (0.12 mole) trichlorosilane and 12.2 g. (0.12 mole) triethylamine in 188 ml. of dry benzene for one hour. Then 3.0 g. (0.012 mole) of 1,2-bis(o-anisylphenylphosphinyl) ethane in 75 ml. of dry acetonitrile was added and the mixture refluxed 1.5 hours. Quenching in 30% sodium hydroxide solution followed by separating and evaporating the organic layer gave 1.4 g. of crude crystals which were insoluble in cold methanol. Further crystallization from hot methanol gave 1,2-bis(o-anisylphenylphosphino) ethane, m.p. 102°-104° C., [α]D20 -83.4° (C=0.5 in CHCl3). The mass spectra gave a very strong parent peak at 458 and the nmr confirmed the structure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04220590 |
| 출처 데이터셋 | uspto-grants-1980_09 |
| ORD ID | ord-393e2fa1622e4648889c7113444d8e50 |
| 출처 메모 | uspto-grants-1980_09 |