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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55935Erstellt: 25. Oktober 2026

Methanol → Methyl 4-(difluoromethoxy)-3-hydroxybenzoate

https://huagongshe.com/reaction/55935

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt4-(Difluoromethoxy)-3-hydroxybenzaldehydeHCID 2758295—
EduktPotassium hydroxy sulfiteHCID 23707502—
ProduktMethyl 4-(difluoromethoxy)-3-hydroxybenzoateHCID 5692662370%

Reaktionsbedingungen

Temperatur52.5 °C

Reaktionsschritte

100 g of 3-hydroxy-4-(difluoromethoxy)-benzaldehyde (0.53 mol) were dissolved in MeOH (600 ml), solid Oxone® (325 g, 1.06 mol) was added portion-wise in 1 hour and solution was stirred and warmed to 50-55° C. for 2 hours. The solvent was concentrated under vacuum to 200 ml and water (1 L) was added. The resulting heterogeneous solution was stirred at 50 to 55° C., then toluene (500 ml) was added, and the biphasic mixture vigorously stirred. Aqueous phase was discharged and the organic one was washed with water (500 ml). Active charcoal (10 g) was added and the organic solution stirred for 20 minutes. It was filtered on a celite pad, the solvent was concentrated under vacuum to 2 to 3 volumes, and the obtained solution was warmed to 80 to 90° C. n-Heptane (400 ml) was slowly added. The mixture was cooled to 0° C. and the suspension was stirred at 0° C. over-night. The solid was filtered on a Buchner funnel and washed with n-heptane (100 ml). The obtained white solid was dried under vacuum at room temperature. (yield 70%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434691B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-f7c06711277f4a31a07b907e1bbac17c
Quellennotizuspto-grants-2016_09