Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1741869Erstellt: 26. Oktober 2026

Methanol → Methyl 2-(3-hydroxyphenoxy)phenylacetate

https://huagongshe.com/reaction/1741869

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktBoron tribromideHCID 25134—
EduktSodium BicarbonateHCID 516892—
EduktMethyl 2-(3-methoxyphenoxy)phenylacetateHCID 14620154—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 2-(3-hydroxyphenoxy)phenylacetateHCID 1462015592,3%

Reaktionsschritte

Boron tribromide (12.89 g, 0.051 mol) was dissolved in dichloromethane (50 ml) and cooled to 0°-5° C. A solution of methyl 2-(3-methoxyphenoxy)phenylacetate (7.0 g; 0,026 mol) in dichloromethane (80 ml) was added dropwise, with stirring over 1 hour. After stirring at 0°-5° C. for 20 minutes the mixture was added dropwise, with stirring to absolute methanol (100 ml) maintaining the temperature at 0°-5° C. The resulting solution was poured into water (250 ml) containing sodium bicarbonate (12 g), and the resulting mixture was extracted with ether (500 mls). The organic phase was washed with water (3×200 ml) and saturated brine (150 ml). After drying and filtration, evaporation of the ether solution gave methyl 2-(3-hydroxyphenoxy)phenylacetate (D) (6.12 g, 92.3% yield) as a brown gum. This material was suitable for use in subsequent steps without further purification. However, chromatography using mixtures of ether and hexane as eluant gave material of higher purity as a viscous golden oil which rapidly darkened on exposure to air.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05334748
Quelldatensatzuspto-grants-1994_08
ORD IDord-1d6383ec4a74413994147ad4017d3b84
Quellennotizuspto-grants-1994_08