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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52340Generated: October 25, 2026

3-Bromo-1,1,1-trifluoro-2-propanone → 2-[4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl]pyridine

https://huagongshe.com/reaction/52340

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-1,1,1-trifluoro-2-propanoneHCID 79008—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178504797HCID 178504797—
SolventIsopropanolHCID 3776—
Product2-[4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl]pyridineHCID 2299798818%

Reaction Steps

To a mixture of the amidine of step 1 (4.4 g, 16 mmol) and sodium bicarbonate (2.7 g, 32 mmol) in isopropanol (400 ml), 3-bromo-1,1,1-trifluoroacetone (2.5 ml, 24 mmol) was added. After heating at 75°-80° C. for 24 hours, the reaction mixture was cooled and filtered. The residue was washed with methylene chloride and the combined organic fractions were dried over sodium sulfate, filtered and concentrated. The crude product (16.2 g) was chromatographed (silica gel, ethyl acetate/toluene 1/1) to give 2-[4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl]pyridine (1.1 g, 18%) as a white solid: mp 195°-198° C. Anal. Calc'd. for C16H14N3SO3F3 : C, 49.87, H, 3.66, N, 10.90. Found: C, 50.13 , H, 3.66, N, 10.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616601
Source datasetuspto-grants-1997_04
ORD IDord-fbf0cb7a972543b0b9de43f5431ab342
Source noteuspto-grants-1997_04