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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730189Generated: October 25, 2026

Ethyl Acetate → Ethyl 1-(3-trifluoromethylbenzyl)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/730189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl indole-2-carboxylateHCID 73125—
Reactant1-(Bromomethyl)-3-(trifluoromethyl)benzeneHCID 123061—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-(3-trifluoromethylbenzyl)-1H-indole-2-carboxylateHCID 6869691488.6%

Reaction Steps

A suspension of 0.492 g (2.6 mmol) of ethyl 1H-indole-2-carboxylate, of 0.683 g (2.86 mmol) of 3-trifluoromethylbenzyl bromide and of 0.898 g (6.5 mmol) of potassium carbonate in 50 ml of dimethylformamide is stirred at 60° C. for 24 hours. The reaction mixture is cooled and is poured into a mixture of ice-cold water and of ethyl acetate. After settling, the organic phase is separated and is then washed with two times 50 ml of water and then with 50 ml of a saturated sodium chloride solution. The solution is dried over magnesium sulfate and filtered, and then the filtrate is concentrated under reduced pressure. 0.8 g of an oil is obtained, which oil is used as is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582671B2
Source datasetuspto-grants-2009_09
ORD IDord-5338d281b80043c1b1598ca4d4aa238d
Source noteuspto-grants-2009_09