Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610408Generated: November 2, 2026

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

https://huagongshe.com/reaction/1610408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantSodium BicarbonateHCID 516892—
Reactant(1RS,2SR)-1-hydroxy-1-(1-naphthalenyl)-3-(4-(trifluoromethyl)phenyl)-2-propylamine hydrochlorideHCID 69553920—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-((1RS,2SR)-2-hydroxy-2-(1-naphthalenyl)-1-((4-(trifluoromethyl)phenyl)methyl)ethyl)cyclohexanecarboxamideHCID 2226193579.4%

Reaction Steps

To a solution of (1RS,2SR)-1-hydroxy-1-(1-naphthalenyl)-3-(4-(trifluoromethyl)phenyl)-2-propylamine hydrochloride (150 mg, 0.39 mmol) in ethyl acetate (5 ml) were added cyclohexanecarbonyl chloride (87.8 ml, 0.59 mmol) and saturated-aqueous sodium hydrogen carbonate (5 ml) and the mixture was stirred overnight at room temperature. The reaction solution was diluted with water (50 ml) and extracted with ethyl acetate (50 ml×2). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) and recrystallized from ethyl acetate-hexane to give the title compound (141 mg, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-6481be03cfb24dbd88a975f63dfe36bb
Source noteuspto-grants-2006_01