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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 550154Erstellt: 27. Oktober 2026

Hydrochloric Acid → 7-(Trifluoromethyl)-1H-indole

https://huagongshe.com/reaction/550154

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBoron trifluoride etherateHCID 8000—
Edukt7-TrifluoromethylisatinHCID 604575—
EduktSodium borohydrideHCID 4311764—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-(Trifluoromethyl)-1H-indoleHCID 10419882—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

To a stirred mixture of 7-trifluoromethyl-1H-indole-2,3-dione (116 mg) in THF (5.00 mL) was added boron trifluoride etherate (0.205 mL, 1.62 mmol) followed by sodium borohydride (71.4 mg, 1.88 mmol). The resulting mixture was stirred at -20° C. for 2 hrs, then water (1 mL) was added and the mixture was stirred at 0° C. for 10 min. The solution was acidified to pH=1 with 2N HCl, warmed to r.t. and stirred at r.t. for 20 min prior to extraction with EtOAc. The extracts were dried over magnesium sulphate, concentrated in vacuo and the residue purified by chromatography over silica gel eluting with hexane to give 7-trifluoromethyl-1H-indole. 1H NMR (400 MHz, CDCl3) δ ppm 6.63-6.68 (1 H, m), 7.20 (1 H, t, J=7.71 Hz), 7.30-7.35 (1 H, m), 7.47 (1 H, d, J=7.33 Hz), 7.83 (1 H, d, J=8.08 Hz), and 8.56 (1 H, br. s.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943767B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-ac421b94dde243209ef42c6a1ae42d70
Quellennotizuspto-grants-2011_05