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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804770Generated: November 1, 2026

Ethanol → 4-Cyclobutylmethoxy-1H-indole-2-carboxylic acid

https://huagongshe.com/reaction/1804770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant4-cyclobutylmethoxy-1H-indole-2-carboxylic acid ethyl esterHCID 66841782—
Product4-Cyclobutylmethoxy-1H-indole-2-carboxylic acidHCID 59152682—

Reaction Steps

The 4-cyclobutylmethoxy-1H-indole-2-carboxylic acid ethyl ester (15a) obtained above is mixed with a 2M-solution of KOH in EtOH (16.9 ml, 33.8 mmol) and stirred for 24 hours. The solvent is then evaporated and the residue is partitioned between water and DCM. The water layer is acidified with HCl and extracted twice with EtOAc. The combined organic layers are washed with brine, dried over anhydrous sodium sulfate, filtered and evaporated to give a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354431B2
Source datasetuspto-grants-2013_01
ORD IDord-bb3d74c65c2d4865905993c75dbda35b
Source noteuspto-grants-2013_01