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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525670Generated: October 26, 2026

Water → Ethyl 4-[[3-chloro-4-(trifluoromethyl)phenoxy]methyl]benzoate

https://huagongshe.com/reaction/1525670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-(bromomethyl)benzoateHCID 954261—
Reactant3-Chloro-4-(trifluoromethyl)phenolHCID 13609147—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductEthyl 4-[[3-chloro-4-(trifluoromethyl)phenoxy]methyl]benzoateHCID 8961918099%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 3-chloro-4-(trifluoromethyl)phenol (110 mg, 0.56 mmol) in DMSO (5.0 mL) was added potassium carbonate (155 mg, 1.1 mmol). The reaction mixture was stirred at room temperature for 10 minutes, before addition of ethyl 4-(bromomethyl)benzoate (136 mg, 0.56 mmol). The resulting mixture was heated to 70° C. with stirring for 3 hours before cooling back to room temperature. Water (50 mL) and EtOAc (50 mL) were added and the layers partitioned. The aqueous layers were washed with EtOAc (2×50 mL) and the combined organic layers dried over magnesium sulfate, filtered and concentrated in vacuo to yield a white solid as the title compound (198 mg, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085517B2
Source datasetuspto-grants-2015_07
ORD IDord-ad9755e10261443b89dc11c2a42b7c2b
Source noteuspto-grants-2015_07