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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1787124Erstellt: 25. Oktober 2026

Dimethyl Sulfate → N-(4-methoxy-2,3,6-trimethylphenyl)formamide

https://huagongshe.com/reaction/1787124

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktN-(4-hydroxy-2,3,6-trimethylphenyl)formamideHCID 21961295—
LösungsmittelMethanolHCID 887—
LösungsmittelPotassium HydroxideHCID 14797—
ProduktN-(4-methoxy-2,3,6-trimethylphenyl)formamideHCID 21961345—

Reaktionsschritte

N-(4-Hydroxy-2,3,6-trimethylphenyl)formamide (30.0 g, 167 mmol) was dissolved in a mixed solvent of 4 N potassium hydroxide aqueous solution (100 mL) and methanol (300 mL), and dimethyl sulfate (42.0 g, 334 mmol) was added to the solution at room temperature and the mixture was heated under reflux for 14 hours. After ice-cooling, the precipitated crystals were collected by filtration to obtain the crude product of N-(4-methoxy-2,3,6-trimethylphenyl)formamide. To a suspension of the compound in methanol (200 mL) was added concentrated hydrochloric acid (50 mL) and the mixture was heated under reflux for 3 hours. The reaction mixture was cooled to room temperature, and then was neutralized with a 8 N aqueous sodium hydroxide solution. The product was twice extracted with ethyl acetate, and the combined extract was washed with 10% sodium hydrosulfite aqueous solution and water, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was crystallized from isopropyl ether to obtain the object compound 21.0 g (yield 76%). Melting point: 70-72° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07507841B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-d581bba9f39d4e5893fa9a5b878182ff
Quellennotizuspto-grants-2009_03