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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480067Generated: October 31, 2026

Tetrahydrofuran → 5-Chloro-3-methyl-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/480067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant1H-Indole-2-carboxylic acid, 5-chloro-3-methyl-, ethyl esterHCID 949859—
SolventMethanolHCID 887—
Product5-Chloro-3-methyl-1H-indole-2-carboxylic acidHCID 3159706—

Reaction Conditions

Temperature25 °C

Reaction Steps

2N NaOH (20 mL) was added to a suspension of 5-chloro-3-methyl-1H-indole-2-carboxylic acid ethyl ester (7.0 g, 29.4 mmol) in methanol (50 mL) and the resulting mixture stirred at 25° C. for 18 hours. Tetrahydrofuran (100 mL) was added and the resulting solution heated at reflux for 30 minutes and concentrated. The residue was dissolved in water and the resulting solution extracted twice with ethyl acetate. The aqueous layer was acidified and the precipitate collected by filtration and washed with water (5.24 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649634B2
Source datasetuspto-grants-2003_11
ORD IDord-f015c50c841643678696f71adf269ac7
Source noteuspto-grants-2003_11