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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1700287Erstellt: 26. Oktober 2026

Sodium borohydride → 3-Cyano-6-((4-methoxybenzyl)oxy)-1-(3-hydroxyprop-2-en-1-yl)benzene

https://huagongshe.com/reaction/1700287

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt3-Cyano-6-((4-methoxybenzyl)oxy)-1-(2-formylethenyl)benzeneHCID 73437155—
LösungsmittelDichloromethane methanol waterHCID 21958822—
Produkt3-Cyano-6-((4-methoxybenzyl)oxy)-1-(3-hydroxyprop-2-en-1-yl)benzeneHCID 700736253.985,7%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To 3-cyano-6-((4-methoxybenzyl)oxy)-1-(2-formylethenyl)benzene (2.30 g) in 100 mL solution of CH2Cl2/MeOH/H2O (2:7:1) was added NaBH4 (0.29 g) at 0° C. The resulting solution was stirred at 0° C. for 1 hour and concentrated. The resulting residue was diluted with 100 mL of saturated aqueous NaHCO3 and extracted with ethyl acetate (3×). The organic layer was dried, concentrated to afford 3-cyano-6-((4-methoxybenzyl)oxy)-1-(3-hydroxyprop-2-en-1-yl)benzene (92.3 g) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06350761B1
Quelldatensatzuspto-grants-2002_02
ORD IDord-84699d1069f149d1b44a43c6f22a0c66
Quellennotizuspto-grants-2002_02