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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091024Generated: October 29, 2026

Hydrochloric Acid → 5-fluoro-N-methoxy-N,3-dimethyl-1-benzofuran-2-carboxamide

https://huagongshe.com/reaction/2091024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Acetyl-4-fluorophenolHCID 95992—
Reactant2-Chloro-N-methoxy-N-methylacetamideHCID 2734716—
SolventDimethylformamideHCID 6228—
Product5-fluoro-N-methoxy-N,3-dimethyl-1-benzofuran-2-carboxamideHCID 5502774528.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 1-(5-fluoro-2-hydroxyphenyl)ethanone (10.0 g), 2-chloro-N-methoxy-N-methylacetamide (9.82 g), sodium iodide (19.5 g) and N,N-dimethylformamide (200 mL) was added potassium carbonate (18.0 g), and the mixture was stirred at 80° C. overnight. 1N Hydrochloric acid was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give a brown solid. To a solution (200 mL) of the obtained solid in N,N-dimethylformamide was added 1,8-diazabicyclo[5.4.0]undec-7-ene (9.71 mL), and the mixture was stirred at 120° C. for 4 hr. 1N Hydrochloric acid was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:3, volume ratio) to give the title object compound (4.37 g, 28%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-33389889aee84fd5a07f48b88e586dbe
Source noteuspto-grants-2013_05