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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2361156Erstellt: 26. Oktober 2026

Dimethyl Sulfate → 4-Benzyloxy-2-methoxy-3-methyl-benzaldehyde

https://huagongshe.com/reaction/2361156

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktSodium HydroxideHCID 14798—
Edukt1,4-DioxaneHCID 31275—
Edukt4-(Benzyloxy)-2-hydroxy-3-methylbenzaldehydeHCID 59761690—
LösungsmittelWaterHCID 962—
Produkt4-Benzyloxy-2-methoxy-3-methyl-benzaldehydeHCID 59761764—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 4-benzyloxy-2-hydroxy-3-methyl-benzaldehyde (1.57 g, 6.49 mmol), dimethylsulfate (1.04 ml, 10.9 mmol), NaOH (1.02 g, 25.5 mmol), 1,4-dioxane (20 mL) and water (10 mL) was stirred at 90° C. for 6 h. The reaction mixture was cooled to RT, water (100 mL) was added, extracted with EtOAc (150 mL). The extract was washed with brine (100 mL), dried over Na2SO4 and evaporated. The residue was purified on SiO2 (25 g) column, hexane to toluene. Yield 1.20 g (4.68 mmol, 72%), white solid. 1H NMR (300 MHz, DMSO): δ 10.11 (s, 1H), 7.64 (d, J=8.9 Hz, 1H), 7.49-7.32 (m, 5H), 7.05 (d, J=8.9 Hz, 1H), 5.24 (s, 2H), 3.81 (s, 3H), 2.14 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08686005B2
Quelldatensatzuspto-grants-2014_04
ORD IDord-21842eb5c9b64303b614181f950273d1
Quellennotizuspto-grants-2014_04