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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2299149Erstellt: 24. Oktober 2026

6-Nitro-2-(trifluoromethyl)-1H-benzimidazole → 5-Amino-2-(trifluoromethyl)benzimidazole

https://huagongshe.com/de/reaction/2299149

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Nitro-2-(trifluoromethyl)-1H-benzimidazoleHCID 67595—
Edukt2-Nitro-1H-benzimidazoleHCID 97234—
Edukt4-Nitro-1,2-phenylenediamineHCID 5111791—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelTrifluoroacetic acidHCID 6422—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-Amino-2-(trifluoromethyl)benzimidazoleHCID 1934580%

Reaktionsschritte

A solution of 4-nitro-1,2-phenylenediamine (3.0 g, 20 mmol) in 15 ml of trifluoroacetic acid was stirred at reflux for 12 h. The reaction mixture was concentrated in vacuo to yield a oily residue, which was dissolved in 100 ml of EtOAc and washed with aqueous NaHCO3. The organic layer was dried over MgSO4 and concentrated in vacuo to provide an oil which was characterized as 2-trifluoromethyl-5-nitrobenzimidazole and subjected to the following reaction without further purification. The nitrobenzimidazole and 500 mg of 10% Pd-C were dissolved in 100 ml of MeOH and stirred for 12 h under H2. The reaction mixture was filtered and concentrated in vacuo, yielding 3.2 g (16 mmol, 80%) of the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06495583B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-ab4002b281cb41b58dbf56acf2212ce5
Quellennotizuspto-grants-2002_12