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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231839Erstellt: 24. Oktober 2026

Benzyl Bromide → 1-benzyl-2-trifluoromethyl-(1H)-indole

https://huagongshe.com/de/reaction/231839

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktSodium hydrideHCID 24758—
Edukt2-(trifluoromethyl)-1H-indoleHCID 10932124—
EduktMonosodium phosphateHCID 23672064—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-benzyl-2-trifluoromethyl-(1H)-indoleHCID 17882580—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

8.6 g of 2-trifluoromethyl-(1H)-indole and 100 ml of tetrahydrofuran were mixed together under an inert atmosphere and cooled to 0° C. Over 15 minutes, about 2.4 g of a suspension of sodium hydride at 50% in oil was added in small fractions and 6.5 ml of benzyl bromide in solution in 10 ml of tetrahydrofuran were introduced over 5 minutes. The mixture was stirred for 42 hours at ambient temperature and then was poured into water saturated with monosodium phosphate. The mixture was extracted with ethyl ether, and the extracts were dried and concentrated to dryness by distillation under reduced pressure. The residue was chromatographed over silica and eluted with a mixture of hexane and ethyl acetate (9/1) to obtain 12.54 g of 1-benzyl-2-trifluoromethyl-(1H)-indole melting at approx. 20° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04849443
Quelldatensatzuspto-grants-1989_07
ORD IDord-6aba9620a94d47ac8f394f06fb33675d
Quellennotizuspto-grants-1989_07