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HRID 33697作成日:2026年10月24日

4-Hydroxybenzaldehyde → 4-Piperidin-1-ylmethyl-phenol

https://huagongshe.com/ja/reaction/33697

反応式

関与物質

役割名称HCID仕込み量
反応物4-HydroxybenzaldehydeHCID 126—
反応物PiperidineHCID 8082—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
溶媒Acetic AcidHCID 176—
生成物4-Piperidin-1-ylmethyl-phenolHCID 11636972—

反応手順

A solution of 4-hydroxybenzaldehyde (10 g), piperidine (8.9 mL), and acetic acid (4.7 mL) in DCE (200 mL) was treated with sodium triacetoxyborohydride (24 g). After 16 h, the resulting mixture was treated with saturated aqueous sodium bicarbonate (100 mL) and extracted with DCM (5×100 mL). The combined organic phases were dried (magnesium sulfate) and evaporated. Trituration of the residue with ethyl acetate gave the title compound as a white crystalline solid (5.5 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429586B2
出典データセットuspto-grants-2008_09
ORD IDord-30552338e6264365b23655f40314d983
出典メモuspto-grants-2008_09