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HRID 1166346Erstellt: 27. Oktober 2026

3-Bromo-1,1,1-trifluoro-2-propanone → 2-(4-methylphenyl)-4-hydroxy-1-(4-(methylsulfonyl)phenyl]-4-trifluoromethyl-4,5-dihydro-1H-imidazole

https://huagongshe.com/reaction/1166346

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Bromo-1,1,1-trifluoro-2-propanoneHCID 79008—
EduktSodium BicarbonateHCID 516892—
EduktHCID 178425632HCID 178425632—
LösungsmittelIsopropanolHCID 3776—
Produkt2-(4-methylphenyl)-4-hydroxy-1-(4-(methylsulfonyl)phenyl]-4-trifluoromethyl-4,5-dihydro-1H-imidazoleHCID 1052490147,3%

Reaktionsbedingungen

Temperatur77.5 °C

Reaktionsschritte

To a mixture of 4-methyl-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Step 1) (5 g, 17.4 mmol) and sodium bicarbonate (2.9 g, 34.7 mmol) in isopropanol (200 mL), 3-bromo-1,1,1-trifluoroacetone (3.6 ml, 34.7 mmol) was added. After heating the reaction mixture at 75-80° C. for 20 hours, the solvent was removed. The residue was redissolved in methylene chloride and washed with water. The organic fractions were combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude mixture (8.9 g) was purified by chromatography (silica gel, toluene/ethyl acetate 6/4) to give 2-(4-methylphenyl)-4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-trifluoromethyl-4,5-dihydro-1H-imidazole (3.28 g, 47%) as a white solid: mp 198-199° C. Anal. Calc'd for C18H17N2F3SO3.0.3 PhMe C, 56.67; H, 4.59; N, 6.58. Found: C, 56.95; H, 4.68; N, 6.13.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06613789B2
Quelldatensatzuspto-grants-2003_09
ORD IDord-cab06c7e9f1e4339ae0299e37321fe38
Quellennotizuspto-grants-2003_09