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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104608Generated: October 29, 2026

Hydrochloric Acid → Ethyl[4-({3-[3-phenyl-8-(trifluoromethyl)quinolin-yl]phenoxy}methyl)phenyl]acetate

https://huagongshe.com/reaction/2104608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-(4-(bromomethyl)phenyl)acetateHCID 15712209—
Reactant3-(3-Phenyl-8-trifluoromethyl-quinolin-4-yl)-phenolHCID 66586292—
SolventDimethylformamideHCID 6228—
ProductEthyl[4-({3-[3-phenyl-8-(trifluoromethyl)quinolin-yl]phenoxy}methyl)phenyl]acetateHCID 13172758738.7%

Reaction Steps

To a solution of 3-[3-phenyl-8-(trifluoromethyl)quinolin-4-yl]phenol (0.178 g, 0.487 mmol), and potassium carbonate (0.134 g, 0.974 mmol), in DMF at 120° C. is added 4-bromomethylphenylacetic acid ethyl ester (0.334 g, 1.46 mmol), drop wise over 2 h. After an additional 2 h, the cooled reaction is poured into 2N aq HCl and extracted with ethyl acetate. The combined extracts are washed with sat aq NaHCO3, water, brine, and dried with magnesium sulfate. The extracts are concentrated and the residue is chromatographed with 1:9 ethyl acetate:hexanes to afford the title compound as a syrup (0.051 g, 37%). MS m/z 542; HRMS: calcd for C33H26NF3O3+H, 542.19430; found (ESI, [M+H]+), 542.194.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576215B2
Source datasetuspto-grants-2009_08
ORD IDord-a63aeddca4254a6388a9235a4eb163c2
Source noteuspto-grants-2009_08