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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 862402Erstellt: 23. Oktober 2026

Water → (2,6-Dimethoxy-4-methylphenyl)(2-methylaminophenyl) Ketone

https://huagongshe.com/de/reaction/862402

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktN-Methylisatoic anhydrideHCID 25160—
Edukt3,5-DimethoxytolueneHCID 77844—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(2,6-Dimethoxy-4-methylphenyl)(2-methylaminophenyl) KetoneHCID 5732221678%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

To a solution of 30 g of 3,5-dimethoxytoluene in 400 ml of tetrahydrofuran are added, at a temperature in the region of -20° C., 129 ml of 1.6M butyllithium in hexane. Once the introduction is complete, the reaction mixture is brought to a temperature of 0° C. and is then stirred for 1 hour. It is cooled to -20° C. and 36.67 g of N-methylisatoic anhydride are added portionwise. The mixture is allowed to return to room temperature and is stirred over 2 hours, followed by addition of 500 ml of water and extraction with ethyl acetate. The organic phase is washed with water, dried over sodium sulphate and evaporated under vacuum. The residue is purified by chromatography on silica gel, eluent: toluene/ethyl acetate 9/1. The fractions of pure product are concentrated under vacuum and the residue is crystallized from isopropyl ether, filtered and dried. Beige crystals melting at 215° C. are obtained; Yield=78%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05719143
Quelldatensatzuspto-grants-1998_02
ORD IDord-47e41d771d9c4d0280e185636e9a06cc
Quellennotizuspto-grants-1998_02