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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344716Generated: October 31, 2026

Ethanol → Ethyl 1H-indole-3-acetate

https://huagongshe.com/reaction/344716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantIndole-3-Acetic AcidHCID 802—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ProductEthyl 1H-indole-3-acetateHCID 1306790%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 5.0 g (28.5 mmols) of indole-3acetic acid, 250 ml of ethanol and 5 ml of conc. sulfuric acid was heated under reflux for 2 hours. After cooling to 0° C., the mixture was neutralized with a 2 normal aqueous sodium hydroxide solution. The solvent was evaporated under reduced pressure, and then water was added to the residue followed by extraction of the solution with chloroform. The chloroform layer was washed with an aqueous saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was dried to afford 5.2 g (yield: 90%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053408
Source datasetuspto-grants-1991_10
ORD IDord-1713a83d80b14f36bfc94b17e470b70f
Source noteuspto-grants-1991_10