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HRID 52755作成日:2026年10月26日

4-(Dimethylamino)Benzaldehyde → 2,6-Di-tert-butyl-4-((4-(dimethylamino)phenyl)(piperidin-1-yl)methyl)phenol

https://huagongshe.com/reaction/52755

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Dimethylamino)BenzaldehydeHCID 7479—
反応物PiperidineHCID 8082—
反応物2,6-Di-tert-butylphenolHCID 31405—
反応物Toluene hexaneHCID 21889329—
溶媒O-XyleneHCID 7237—
生成物2,6-Di-tert-butyl-4-((4-(dimethylamino)phenyl)(piperidin-1-yl)methyl)phenolHCID 4066737—

反応手順

To 30.4 g (0.2 mol) of 4-dimethylaminobenzaldehyde in 100 ml of xylene, 39.1 g (0.46 mol) of piperidine is added dropwise over a period of six minutes. The mixture is heated at reflux using a Dean-Stark trap until the separation of water is complete. To the cooled reaction mixture 40.3 (0.2 mol) of 2,6-di-tert-butylphenol in 70 ml of xylene is added rapidly. The mixture is then heated at reflux for five hours. The title compound is isolated as an almost white solid by evaporation of the solvent and recrystallization from toluene-hexane. The yield is 66.3 g of the title compound, melting at 184°-185° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616774
出典データセットuspto-grants-1997_04
ORD IDord-beb031635aaa49749c8a2909d1afb736
出典メモuspto-grants-1997_04