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N-Phenylmaleimide → 3-(3,5-Di-tert-butyl-4-hydroxyphenyl)-1-phenylpyrrolidine-2,5-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-Phenylmaleimide | HCID 13662 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-(3,5-Di-tert-butyl-4-hydroxyphenyl)-1-phenylpyrrolidine-2,5-dione | HCID 14148372 | 2.1% |
反応手順
This compound is prepared by the procedure of Example 1 from 2.40 g (0.1 mol) of sodium hydride, 20.63 g (0.1 mol) of 2,6-di-tert-butylphenol, and 17.32 g (0.1 mol) of N-phenylmaleimide in tetrahydrofuran. The reaction mixture is concentrated in vacuo and the residue is dissolved in 150 ml of toluene. The toluene solution is extracted sequentially with 1M sodium hydroxide (2×100 ml) and water (2×50 ml). The organic phase is dried over anhydrous sodium sulfate and then the solvent is removed in vacuo. The residue is triturated with petroleum ether to give 0.78 g (2%) of white crystals: mp 204° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04709050 |
| 出典データセット | uspto-grants-1987_11 |
| ORD ID | ord-c2d334ca504d491ba5ca09fb968575eb |
| 出典メモ | uspto-grants-1987_11 |