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HRID 522485作成日:2026年10月23日

Formaldehyde → 4-(4-Methyl-1-piperazinyl)phenol

https://huagongshe.com/ja/reaction/522485

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物p-(1-Piperazinyl)phenolHCID 92467—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒Acetic acid tetrahydrofuranHCID 23444217—
生成物4-(4-Methyl-1-piperazinyl)phenolHCID 11622486106.4%

反応手順

4-(piperazin-1-yl)phenol 2 g (11.24 mmol) and formaldehyde 4.5 mL (37% in water, 56 mmol) were suspended in a mixture of THF/AcOH 5/1 and let under stirring at room temperature. After 30 minutes sodium triacetoxyborohydride 4.7 g (22.5 mmol) was added portion-wise. The reaction was let stir a few hours and evaporated down. The crude was purified on silica gel with AcOEt/EtOH/(NH3 7 N in MeOH) 8/2/0.2 to give 2.3 g of pink solid as a free base.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09333205B2
出典データセットuspto-grants-2016_05
ORD IDord-4ec99b628aaf4feb9ef037415756c670
出典メモuspto-grants-2016_05