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HRID 271635作成日:2026年10月27日

Allyl Alcohol → 3-(4-(Hydroxymethyl)phenyl)propanal

https://huagongshe.com/reaction/271635

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl AlcoholHCID 7858—
反応物Ethyl AcetateHCID 8857—
反応物4-Iodobenzyl alcoholHCID 29012—
反応物Sodium BicarbonateHCID 516892—
触媒palladium(II) acetateHCID 167845—
触媒Tetrabutylammonium chloride hydrateHCID 16212273—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-(4-(Hydroxymethyl)phenyl)propanalHCID 53425276—

反応条件

温度60 °C

反応手順

10.5 mL (152.8 mmol) allylalcohol, 18.8 g (62.2 mmol) Tetrabutylammonium chloride monohydrate, 12.8 g (152.8 mmol) NaHCO3 and 0.75 g (3.1 mmol) Pd(OAc)2 is added to a solution of 15.0 g (62.2 mmol) 4-iodobenzylalcohol in 100 mL DMF at RT under an N2 atmosphere and the reaction solution is heated to 60° C. for 3 h. The solvent is eliminated i.vac., the residue combined with 250 mL EtOAc and 80 mL water and suction filtered through a fibreglass filter. 80 mL NaCl solution are added to the filtrate, the phases are separated and the organic phase is dried over MgSO4. After the desiccant and solvent have been eliminated the residue is purified by column chromatography on silica gel (gradient: cyc/EtOAc 3:1 after cyc/EtOAc 1:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452911B2
出典データセットuspto-grants-2008_11
ORD IDord-c091aec98fb744dc835629a691d3c1bb
出典メモuspto-grants-2008_11