Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 429571Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/429571

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
PatentnummerUS06316637B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-608787df50804d9f8286080e62b98460
Quellennotizuspto-grants-2001_11