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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355691Generated: October 29, 2026

Trifluoroacetic acid → ethyl 1-(2-carboxyethyl)-4-methyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/355691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantethyl 1-(2-tert-butoxycarbonylethyl)-4-methyl-1H-indole-2-carboxylateHCID 15548944—
SolventDichloromethaneHCID 6344—
Productethyl 1-(2-carboxyethyl)-4-methyl-1H-indole-2-carboxylateHCID 1554894599.4%

Reaction Steps

A mixture of ethyl 1-(2-tert-butoxycarbonylethyl)-4-methyl-1H-indole-2-carboxylate (3.76 g, 11.4 mmol), trifluoroacetic acid (14.8 g, 130 mmol) and dichloromethane (50 ml) was stirred at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure and water was added to the residue, followed by extraction with diethyl ether (three times). The extract solution was washed with a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain ethyl 1-(2-carboxyethyl)-4-methyl-1H-indole-2-carboxylate (3.12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834454
Source datasetuspto-grants-1998_11
ORD IDord-ea919e47a4784f73b6cc92e6726e5b6c
Source noteuspto-grants-1998_11