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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730193Generated: October 26, 2026

Water → Ethyl 1-(3-isopropylphenyl)-5-trifluoromethyloxy-1H-indole-2-carboxylate

https://huagongshe.com/reaction/730193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactantethyl 5-(trifluoromethoxy)-1H-indole-2-carboxylateHCID 2737230—
Reactant3-Isopropylbenzeneboronic acidHCID 2773478—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
ProductEthyl 1-(3-isopropylphenyl)-5-trifluoromethyloxy-1H-indole-2-carboxylateHCID 6869888235%

Reaction Steps

A mixture of 0.2 g (0.73 mmol) of ethyl 5-trifluoromethyloxy-1H-indole-2-carboxylate, of 0.24 g (1.46 mmol) of 3-isopropylphenylboronic acid, of 0.2 g (1.1 mmol) of copper diacetate and of 0.12 ml (1.46 mmol) of pyridine in 5 ml of dichloromethane is stirred in the presence of 4 Å molecular sieve at ambient temperature for 4 days. The mixture is poured onto 100 ml of water and 50 ml of dichloromethane. The organic phase is separated, washed with 1N hydrochloric acid, dried over magnesium sulfate and then concentrated under reduced pressure. The residue is purified by chromatography on a silica column, elution being carried out with a mixture of cyclohexane and of ethyl acetate. 0.1 g of product is obtained, which product 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-d6264267eb6b4d9192a05dbc7abb6817
Source noteuspto-grants-2009_09