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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726716Generated: November 2, 2026

Methanol → methyl 1H-indole-4-carboxylate

https://huagongshe.com/reaction/1726716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantIndole-4-carboxylic acidHCID 595229—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDichloromethaneHCID 6344—
Productmethyl 1H-indole-4-carboxylateHCID 273366879%

Reaction Steps

N,N-Dimethylaminopyridine (7.6 mg, 0.06 mmol) was added to a mixture of 1H-indole-4-carboxylic acid (100 mg, 0.62 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (131 mg, 0.68 mmol), and methanol (1 mL, 24.7 mmol) in dichloromethane (2 mL). The mixture was allowed to stir at room temperature overnight, then the solvent was evaporated and ethyl acetate (20 mL) was added. The solution was washed with 1 M HCl (2×15 mL), saturated sodium hydrogen carbonate (15 mL) and brine (10 mL), dried (MgSO4), filtered and evaporated to give 1H-indole-4-carboxylic acid, methyl ester (85.4 mg, 79%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491741B2
Source datasetuspto-grants-2009_02
ORD IDord-5e4e54d7332d417495aa7356e5cc629f
Source noteuspto-grants-2009_02