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HRID 247614作成日:2026年10月26日

N-Phenylmaleimide → 3-(3,5-Di-tert-butyl-4-hydroxyphenyl)-1-phenylpyrrolidine-2,5-dione

https://huagongshe.com/reaction/247614

反応式

関与物質

役割名称HCID仕込み量
反応物N-PhenylmaleimideHCID 13662—
反応物Sodium hydrideHCID 24758—
反応物2,6-Di-tert-butylphenolHCID 31405—
溶媒TetrahydrofuranHCID 8028—
生成物3-(3,5-Di-tert-butyl-4-hydroxyphenyl)-1-phenylpyrrolidine-2,5-dioneHCID 141483722.1%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04709050
出典データセットuspto-grants-1987_11
ORD IDord-c2d334ca504d491ba5ca09fb968575eb
出典メモuspto-grants-1987_11