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1,2-Bis(dichlorophosphino)benzene → 1,2-Bis(bis(3,5-diisopropylphenyl)phosphino)benzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2-Bis(dichlorophosphino)benzene | HCID 3316562 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | 3,5-Diisopropylbromobenzene | HCID 11630091 | — |
| 反応物 | HCID 178439359 | HCID 178439359 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1,2-Bis(bis(3,5-diisopropylphenyl)phosphino)benzene | HCID 86654812 | 74% |
反応手順
3,5-Diisopropylbromobenzene (3.04 g, 12.60 mmol) was added dropwise to magnesium (0.48 g, 19.75 mmol) and THF (7 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-diisopropylphenylmagnesium bromide, and 1,2-bis(dichlorophosphino)benzene (0.45 g, 1.61 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 yellow oily substance (1.18 g, yield 74%).
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-1e1949f1d47f4a6da13f1bcaf480c786 |
| 出典メモ | uspto-grants-2014_01 |