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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 505630Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/505630

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPyridineHCID 1049—
Eduktethyl 5-(trifluoromethoxy)-1H-indole-2-carboxylateHCID 2737230—
Edukt3-Isopropylbenzeneboronic acidHCID 2773478—
KatalysatorCupric acetateHCID 8895—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 1-(3-isopropylphenyl)-5-trifluoromethyloxy-1H-indole-2-carboxylateHCID 6869888235%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07781477B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-92ce70887862486b9c6ac3d16176b4a8
Quellennotizuspto-grants-2010_08