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Benzene → 1,2-Bis(o-anisylphenylphosphino) ethane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzene | HCID 241 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Trichlorosilane | HCID 24811 | — |
| 反応物 | 1,2-Bis(o-anisylphenylphosphinyl) ethane | HCID 86734501 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1,2-Bis(o-anisylphenylphosphino) ethane | HCID 15061558 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04142992 |
| 出典データセット | uspto-grants-1979_03 |
| ORD ID | ord-57e71f35f7214d6da13abd879da00e45 |
| 出典メモ | uspto-grants-1979_03 |