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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474622Generated: October 30, 2026

3-(Trifluoromethyl)phenol → Benzonitrile, 5-formyl-2-[3-(trifluoromethyl)phenoxy]-

https://huagongshe.com/reaction/474622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-5-formylbenzonitrileHCID 2769582—
SolventDimethyl SulfoxideHCID 679—
ProductBenzonitrile, 5-formyl-2-[3-(trifluoromethyl)phenoxy]-HCID 8666620341.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-fluoro-5-formylbenzonitrile (1.0 g, 6.71 mmol), 3-(trifluoromethyl) phenol (1.087 g, 6.71 mmol), K2CO3 (2.78 g, 20.12 mmol) in DMSO (20 mL) was heated at 100° C. overnight. After cooling to room temperature, the mixture was partitioned between EA (100 mL) and water (100 mL), the aqueous layer was extracted with EA (50 mL) twice. The combine the organic layers were washed with water, brine and dried over sodium sulfate, filtered, concentrated and purified via flash chromatography to afford the title compound (820 mg, 2.79 mmol, 41.6% yield). LCMS: rt=3.33 min, [M+H+]=292

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-33df72a99035420b996cc10c19113c25
Source noteuspto-grants-2014_01