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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231835Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-trifluoromethyl-3-formyl-(1H)-indole

https://huagongshe.com/reaction/231835

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBis(dichloromethyl) etherHCID 558102—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt2-(trifluoromethyl)-1H-indoleHCID 10932124—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelNitromethaneHCID 6375—
Produkt2-trifluoromethyl-3-formyl-(1H)-indoleHCID 20032128—

Reaktionsbedingungen

Temperatur-65 °C

Reaktionsschritte

6.1 g of aluminum chloride and 20 ml of methylene chloride were mixed together at -65° C. under an inert atmosphere and a solution of 4.61 g of 2-trifluoromethyl-(1H)-indole (J. Org. Chem., 1974 Vol. 39, p. 1836), 1.4 ml of nitromethane and 20 ml of methylene chloride were added at -60° C. 3.3 ml of dichloromethyl ether in solution in 10 ml of methylene chloride were added to the suspension of the resulting mixture was stirred for 15 minutes at -65° C. The temperature was allowed to rise and at about -10° C., a strong evolution of hydrochloric acid was observed which ceased at about 0° C. The black solution obtained was stirred for 30 minutes at 25° C. and the reaction mixture was poured into water and extracted with methylene chloride. The organic phases were washed with an aqueous solution of sodium bicarbonate, then with water and concentrated to dryness under reduced pressure to obtain 4.6 g of 2-trifluoromethyl-3-formyl-(1H)-indole.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04849443
Quelldatensatzuspto-grants-1989_07
ORD IDord-887274cc264541c98dd0abbc446296c2
Quellennotizuspto-grants-1989_07