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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21256Erstellt: 24. Oktober 2026

Chloromethyl Methyl Ether → 3-Chloro-4-methoxymethoxybenzoic acid

https://huagongshe.com/de/reaction/21256

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloromethyl Methyl EtherHCID 7864—
EduktPotassium HydroxideHCID 14797—
Edukt3-Chloro-4-hydroxybenzoic acidHCID 19860—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Chloro-4-methoxymethoxybenzoic acidHCID 5798668895,1%

Reaktionsschritte

3-Chloro-4-hydroxybenzoic acid 0.5 hydrate (2.00 g, 11.6 mmol) was suspended in dichloromethane (50 mL), and the suspension was added with diisopropylethylamine (8.10 mL, 46.5 mmol) and chloromethyl methyl ether (1.80 mL, 23.7 mmol), under ice-cooling. The reaction mixture was warmed to room temperature and stirred for 1.5 hours. The reaction mixture was added with chloromethyl methyl ether (0.45 mL, 5.92 mmol) under ice-cooling, and stirred at room temperature for 1.5 hours. The reaction mixture was added with methanol (100 mL) and 4 mol/L aqueous potassium hydroxide solution (50 mL) and stirred at room temperature for 18 hours. The solvent was evaporated under reduced pressure, and the residue was added with 4 mol/L hydrochloric acid and water, followed by extracting with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to obtain 3-chloro-4-methoxymethoxybenzoic acid (2.39 g, yield 95%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-98ca684b2d7041bc8d3afabb280632b7
Quellennotizuspto-grants-2010_06