化工社化工社 化学情報印刷レポート · 研究参考用
1-Bromo-3,5-di-tert-butylbenzene → 1,2-Bis(bis(3,5-di-tert-butylphenyl)phosphaneyl)benzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Bromo-3,5-di-tert-butylbenzene | HCID 620136 | — |
| 反応物 | 1,2-Bis(dichlorophosphino)benzene | HCID 3316562 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | HCID 178441125 | HCID 178441125 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1,2-Bis(bis(3,5-di-tert-butylphenyl)phosphaneyl)benzene | HCID 56646869 | — |
反応手順
3,5-Di-tert-butylbromobenzene (12.50 g, 46.43 mmol) was added dropwise to magnesium (1.70 g, 69.96 mmol) and THF (50 mL) in an argon atmosphere. After the dropwise addition, the mixture was heated under reflux for 1 hour. The reaction mixture was cooled to ambient temperature and filtered, and the thus-obtained THF solution of 3,5-di-tert-butylphenylmagnesium bromide, and 1,2-bis(dichlorophosphino)benzene (2.00 g, 7.15 mmol) were reacted as in Production Example 1. The reaction was allowed to proceed overnight at 60° C. After purification, the title compound was obtained as a white powder (4.66 g, yield 73%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08637710B2 |
| 出典データセット | uspto-grants-2014_01 |
| ORD ID | ord-4b3913e785514510b517fe3b1864b195 |
| 出典メモ | uspto-grants-2014_01 |