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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610479Generated: November 1, 2026

Cyclohexanecarbonyl chloride → N-((1RS,2SR)-1-((4-fluorophenyl)methyl)-2-hydroxy-2-(4-(trifluoromethyl)phenyl)ethyl)cyclohexanecarboxamide

https://huagongshe.com/reaction/1610479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantSodium BicarbonateHCID 516892—
Reactant(1RS,2SR)-2-amino-3-(4-fluorophenyl)-1-(4-(trifluoromethyl)phenyl)-1-propanolHCID 22261902—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-((1RS,2SR)-1-((4-fluorophenyl)methyl)-2-hydroxy-2-(4-(trifluoromethyl)phenyl)ethyl)cyclohexanecarboxamideHCID 2226216590.2%

Reaction Steps

To a solution of (1RS,2SR)-2-amino-3-(4-fluorophenyl)-1-(4-(trifluoromethyl)phenyl)-1-propanol (450 mg, 1.44 mmol) in ethyl acetate (15 ml) were added cyclohexanecarbonyl chloride (288 ml, 2.15 mmol) and saturated aqueous sodium hydrogen carbonate (15 ml), and the mixture was stirred at room temperature for 3 hrs. The reaction solution was diluted with water (100 ml) and extracted with ethyl acetate (100 ml×2). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. Recrystallization of the residue from ethyl acetate-hexane gave the title compound (550 mg, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-971279da0179492b82c45a4942317c55
Source noteuspto-grants-2006_01