Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1521Erstellt: 24. Oktober 2026

Methyl 5-(benzyloxy)-2-hydroxybenzoate → 4-(Benzyloxy)-2-(hydroxymethyl)phenol

https://huagongshe.com/de/reaction/1521

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 5-(benzyloxy)-2-hydroxybenzoateHCID 13026913—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(Benzyloxy)-2-(hydroxymethyl)phenolHCID 19690921—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Lithium aluminium hydride (0.235 g, 6.2 mMol) was suspended in tetrahydrofuran (25 ml) and cooled to 0° C. 5-Benzyloxy-2-hydroxy benzoic acid methyl ester (2 g, 7.75 mMol) in tetrahydrofuran (10 ml) was added dropwise, via cannula. The mixture was warmed to room temperature and stirred for 20 minutes. The reaction was then cooled to 0° C. and cautiously quenched by the addition of water (0.5 ml), 2M sodium hydroxide solution (0.5 ml), and water (1 ml). The resulting mixture was stirred at room temperature for 30 minutes and filtered. The filtrate was evaporated in vacuo to yield 4-benzyloxy-2-hydroxymethyl phenol as a clear oil which was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726165
Quelldatensatzuspto-grants-1998_03
ORD IDord-d01bdcbca7ae4670b375df3584280165
Quellennotizuspto-grants-1998_03