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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323462Erstellt: 25. Oktober 2026

Iodoethane → 3,4-Dimethoxy-5-ethoxybenzoic Acid

https://huagongshe.com/reaction/323462

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethaneHCID 6340—
EduktPotassium CarbonateHCID 11430—
EduktPotassium HydroxideHCID 14797—
Edukt3-Hydroxy-4,5-Dimethoxybenzoic AcidHCID 74709—
LösungsmittelAcetoneHCID 180—
LösungsmittelEthanolHCID 702—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt3,4-Dimethoxy-5-ethoxybenzoic AcidHCID 18464538—

Reaktionsschritte

Combine 3,4-dimethoxy-5-hydroxybenzoic acid (1.0 g, 5.0 mmol), potassium carbonate (4.2 g, 30.2 mmol), and ethyl iodide (3.9 g, 25.2 mmol) in acetone (50 mL). Heat to reflux. After 24 hours, cool, add methanol (25 mL) and water (5 mL) After 18 hours, concentrate in vacuo to give a residue. Combine the residue and ethanol (50 mL) and potassium hydroxide (0.56 g, 10 mmol). After 18 hours, concentrate in vacuo to give a residue. Partition the residue between ethyl acetate and a 1 M aqueous solution of hydrochloric acid. Extract the aqueous layer three times with ethyl acetate. Combine the organic layers, dry over Na2SO4, filter, and concentrate in vacuo to give a residue. Triturate the residue to give a solid. Collect the solid to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211199B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-3036a5326d3f4426b39da47486114bac
Quellennotizuspto-grants-2001_04