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HRID 853834Erstellt: 24. Oktober 2026

Dimethylformamide → 1-(5,6-Dichloro-benzimidazol-1-yl)-3,3-dimethyl-butan-2-ol

https://huagongshe.com/de/reaction/853834

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
Edukt2-tert-ButyloxiraneHCID 92174—
Edukt5,6-Dichloro-1H-benzimidazoleHCID 331775—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(5,6-Dichloro-benzimidazol-1-yl)-3,3-dimethyl-butan-2-olHCID 5893263473,3%

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

A large (2-5 mL) microwave reactor flask was charged with 5,6-dichlorobenzimidazole (571 mg, 3.1 mmol), 1,2-epoxy-3,3-dimethylbutane (307 mg, 3.1 mmol), powdered anhydrous potassium carbonate (424 mg, 3.1 mmol) and DMF (1.5 mL). The reaction was then heated in a microwave reactor for 6 minutes at 160° C. The reaction was then diluted with ethyl acetate and extracted with water three times. The organics were dried over MgSO4 and the solvent was removed. The residue was crystallized from CH2Cl2 to afford 653 mg (73%) of product as a white solid: 1H NMR (DMSO, 400 MHz) δ 1.06 (s, 9H), 3.47 (dd, 1H, J=2.0, J2=10.4), 4.08 (dd, 1H, J1=10.5, J2=14.4), 4.47 (dd, 1H, J1=2.0, J2=14.4), 7.75 (s, 1H), 7.79 (s, 1H), 8.23 (s, 1H); HPLC-MS calcd. for C21H22Cl2N4O2 (M+H+) 287.1, found 287.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07256207B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-b0e6f8f091394914b5c91aaf2ba37a13
Quellennotizuspto-grants-2007_08