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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230455Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-(2,2,2-Trifluoro-1-hydroxy-ethyl)-6-trifluoromethyl-1H-benzimidazole-5-carbonitrile

https://huagongshe.com/de/reaction/230455

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt3,3,3-Trifluoro-2-hydroxypropanoic acidHCID 244896—
EduktSodium BicarbonateHCID 516892—
Edukt4,5-Diamino-2-(trifluoromethyl)benzonitrileHCID 52991926—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(2,2,2-Trifluoro-1-hydroxy-ethyl)-6-trifluoromethyl-1H-benzimidazole-5-carbonitrileHCID 86635047—

Reaktionsbedingungen

Temperatur108 °C

Reaktionsschritte

4,5-Diamino-2-trifluoromethyl-benzonitrile (4.14 g; 20.6 mmoles) and 3,3,3-trifluoro-2-hydroxy-propionic acid (4.50 g; 31.2 mmoles) were suspended in 6N HCl (7 mL; 42 mmoles) under a nitrogen atmosphere. The reaction was stirred vigorously and heated to 108° C. for 18 hrs, then cooled to room temperature. The reaction was diluted with water (100 mL) and with ethyl acetate (100 mL), then sodium bicarbonate (5.19 g; 62.0 mmoles) was added slowly and in portions to quench the reaction. The aqueous layer was separated and extracted with ethyl acetate (3×40 mL). The extracts were combined, washed with water (30 mL) and brine (30 mL), then dried over Na2SO4. The filtrate was concentrated in vacuo to yield a crude dark solid which was then purified by column chromatography (SiO2; 30% ethyl acetate/CH2Cl2) to yield the title compound as a dark brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07566733B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-c18a7d1784284cc087d5396fc1692a5b
Quellennotizuspto-grants-2009_07