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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 271635Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/271635

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAllyl AlcoholHCID 7858—
EduktEthyl AcetateHCID 8857—
Edukt4-Iodobenzyl alcoholHCID 29012—
EduktSodium BicarbonateHCID 516892—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorTetrabutylammonium chloride hydrateHCID 16212273—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(4-(Hydroxymethyl)phenyl)propanalHCID 53425276—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07452911B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-c091aec98fb744dc835629a691d3c1bb
Quellennotizuspto-grants-2008_11