Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960411Generated: October 26, 2026

Citric Acid → 5-(2-methoxyethoxy)-7-nitro-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/1960411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactantethyl 5-(2-methoxyethoxy)-7-nitro-1H-indole-2-carboxylateHCID 57476190—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product5-(2-methoxyethoxy)-7-nitro-1H-indole-2-carboxylic acidHCID 5747621997.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

Ethyl 5-(2-methoxyethoxy)-7-nitro-1H-indole-2-carboxylate (7.7 g) was dissolved in a mixed solvent of ethanol (75 mL) and tetrahydrofuran (75 mL), 1N aqueous sodium hydroxide solution (75 mL) was added to this solution, and the mixture was stirred at 50° C. for 1.5 hr. Aqueous citric acid solution was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, dried over magnesium sulfate, and filtrated, and the filtrate was concentrated under reduced pressure. The obtained crude product was crystallized from ethyl acetate-hexane to give the title compound (6.8 g, yield 97%) as yellow crystals. melting point 192-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410087B2
Source datasetuspto-grants-2013_04
ORD IDord-4cf0da4ced314d8c862ac4e5269328e6
Source noteuspto-grants-2013_04