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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238882Erstellt: 26. Oktober 2026

Dimethylformamide → Benzamide,4-fluoro-N-methoxy-N-methyl-3-(1-methylethoxy)-

https://huagongshe.com/reaction/238882

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktIsopropyl iodideHCID 6362—
EduktCesium carbonateHCID 10796—
Edukt4-fluoro-3-hydroxy-N-methoxy-N-methylbenzamideHCID 59459052—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzamide,4-fluoro-N-methoxy-N-methyl-3-(1-methylethoxy)-HCID 59459043100%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A 2 L round bottom flask equipped with a mechanical stirrer, a N2 inlet, a condenser and a temperature controller, was charged 4-fluoro-3-hydroxy-N-methoxy-N-methylbenzamide (99.6 g, 0.5 mol), isopropyl iodide (110.5 g, 0.65 mol) and Cs2CO3 (195.5 g) and DMF (300 mL). The reaction mixture was heated at 50° C. for 3 h. Isopropyl iodide (17.0 g, 0.1 mol) was added and the reaction was heated at 50° C. for 12 h. The reaction mixture was allowed to cool to rt and water (1 L) and CH2Cl2 (500 mL) were added. The reaction mixture was stirred at rt for 0.5 h, and the organic phase was separated. The aqueous layer was extracted with CH2Cl2 (3×500 mL). The combined organic extracts were washed with water (2×1 L), brine (1 L), dried over MgSO4, filtered and concentrated in vacuo at 40° C. for 18 h to give 4-fluoro-3-isopropoxy-N-methoxy-N-methlbenzamide as an off-white solid (120.0 g, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642576B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-f5ebc7c24b174f80a0f49481552bd4ea
Quellennotizuspto-grants-2014_02