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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573091Generated: October 26, 2026

Acetic acid, azido-, ethyl ester → methyl 6-fluoro-4-methoxy-1H-indole-2-carboxylate

https://huagongshe.com/reaction/573091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
Reactant4-Fluoro-2-methoxybenzaldehydeHCID 2774537—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Productmethyl 6-fluoro-4-methoxy-1H-indole-2-carboxylateHCID 67227532—

Reaction Conditions

Temperature-20 °C

Reaction Steps

Sodium methoxide solution (25% by weight in methanol, 22.25 mL) and methanol (52 mL) were added to a flask and cooled to −20° C. using an acetonitrile/dry ice bath. Ethyl 2-azidoacetate (25% by weight in ethanol, 50.3 g) and 4-fluoro-2-methoxybenzaldehyde (5.00 g, dissolved in ethyl 2-azidoacetate solution) were added drop-wise to the stirring sodium methoxide solution at −20° C. The solution was then stirred at −20° C. for 3.5 hours, then at 0° C. for one hour. The solution was poured over ice, vacuum filtered, and washed with water. The filtered solid was taken up in xylenes (100 mL), washed twice with brine, and dried using anhydrous sodium sulfate and filtered. In a separate flask xylenes (50 mL) was brought to reflux. The xylene solution containing the filtered material was added drop-wise to the refluxing xylenes. The solution was then refluxed for five hours, cooled, and placed in a freezer for 16 hours. The precipitate was filtered out. The volume of the filtrate was reduced on vacuum to generate a second crop of precipitate, which was washed with hexanes, then 5% ethyl acetate in hexanes and combined with material from the first filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029404B2
Source datasetuspto-grants-2015_05
ORD IDord-16ddcd6ce206484d939357d20c2c7408
Source noteuspto-grants-2015_05