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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104599Generated: October 30, 2026

Sodium Bicarbonate → 4-Phenyl-3-(1-phenylcyclopropyl)-8-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/2104599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-(1-Phenylcyclopropyl)ethanolHCID 13640313—
ReactantHCID 21555860HCID 21555860—
ReactantHCID 178418287HCID 178418287—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product4-Phenyl-3-(1-phenylcyclopropyl)-8-(trifluoromethyl)quinolineHCID 6691329117%

Reaction Conditions

Temperature120 °C

Reaction Steps

Pyridinium chlorochromate (0.417 g, 1.94 mmol) in CH2Cl2 (3 mL) is treated with a mixture of 2-(1-phenylcyclopropyl)ethanol (0.157 g, 0.967 mmol) in CH2Cl2 (2 mL) for 2 h. The reaction is filtered through Celite, treated with AcOH (3 mL) and [2-amino-3-(trifluoromethyl)phenyl](phenyl)methanone (0.128 g, 0.484 mmol), and the methylene chloride is removed in vacuo. Then 1:20H2SO4:AcOH (0.1 mL) is added and the reaction is heated at 120° C. for 3.5 h. The cooled reaction is poured into saturated aq sodium bicarbonate and extracted with ethyl acetate. The extract is washed with saturated aq sodium bicarbonate and dried (MgSO4). The residue is chromatographed eluting with 5:95 ethyl acetate:hexane and then prep HPLC with a gradient of 10-100% acetonitrile/water to afford the title compound (0.032 g). HRMS: calcd for C25H18F3N+H, 390.14696; found (ESI, [M+H]+), 390.1468.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576215B2
Source datasetuspto-grants-2009_08
ORD IDord-9ebad7db2ce2473fbdd434ca636c7445
Source noteuspto-grants-2009_08