戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 613958作成日:2026年10月26日

Benzene → 1,2-Bis(o-anisylphenylphosphino) ethane

https://huagongshe.com/reaction/613958

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物TriethylamineHCID 8471—
反応物TrichlorosilaneHCID 24811—
反応物1,2-Bis(o-anisylphenylphosphinyl) ethaneHCID 86734501—
溶媒MethanolHCID 887—
溶媒AcetonitrileHCID 6342—
生成物1,2-Bis(o-anisylphenylphosphino) ethaneHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04142992
出典データセットuspto-grants-1979_03
ORD IDord-57e71f35f7214d6da13abd879da00e45
出典メモuspto-grants-1979_03