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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5606Generated: October 29, 2026

Ethyl chloroformate → Ethyl alpha-[3(trifluoromethyl)-benzylamino]-1-ethoxycarbonyl-indole-3-acetate hydrochloride

https://huagongshe.com/reaction/5606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantSodium hydrideHCID 24758—
ReactantHCID 19796625HCID 19796625—
SolventDimethylformamideHCID 6228—
ProductEthyl alpha-[3(trifluoromethyl)-benzylamino]-1-ethoxycarbonyl-indole-3-acetate hydrochlorideHCID 1979659566.4%

Reaction Steps

To a magnetically stirred solution of ethyl α-[3(trifluoromethyl)-benzylamino]-indole-3-acetate (1.00 g, 2.66 mmol) in 15 mL of DMF was added under nitrogen 0.112 g (2.79 mmol) of sodium hydride (60% oil dispersion). After stirring at room temperature for 10 minutes, 0.26 ml (2.79 mmol) of ethyl chloroformate was added. Stirring was continued for two hours at room temperature. At the end of this time, the reaction contents were poured into ice water, the aqueous solution extracted with ether and the ether solution washed with saturated brine and dried over anhydrous Na2SO4. Removal of the solvent in vacuo gave the crude product which was chromatographed with 80 g of silica gel using hexane-ethyl acetate (4:1) to yield 0.857 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245046
Source datasetuspto-grants-1993_09
ORD IDord-37e9705164da464eb5088a85a9aeda49
Source noteuspto-grants-1993_09