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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712847Generated: October 26, 2026

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

https://huagongshe.com/reaction/1712847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantIsopropyl iodideHCID 6362—
ReactantCesium carbonateHCID 10796—
Reactant4-fluoro-3-hydroxy-N-methoxy-N-methylbenzamideHCID 59459052—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductBenzamide,4-fluoro-N-methoxy-N-methyl-3-(1-methylethoxy)-HCID 59459043100%

Reaction Conditions

Temperature50 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790770B2
Source datasetuspto-grants-2010_09
ORD IDord-b174e71334a9480499993da7f1bfedbb
Source noteuspto-grants-2010_09