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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474583Generated: October 30, 2026

3-(Trifluoromethyl)phenol → 4-(3-(Trifluoromethyl)phenoxy)benzaldehyde

https://huagongshe.com/reaction/474583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzaldehydeHCID 68023—
SolventDimethylformamideHCID 6228—
Product4-(3-(Trifluoromethyl)phenoxy)benzaldehydeHCID 1214878885.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

K2CO3 (23.45 g, 170 mmol) was added to a solution of 3-(trifluoromethyl)phenol (25 g, 154 mmol) and 4-fluorobenzaldehyde (19.14 g, 154 mmol) in DMF (300 mL), and the reaction mixture was stirred at 140° C. for 4 h. After cooling down to room temperature, the reaction mixture was poured into ice water (2500 ml), extracted with ethyl acetate (500 ml×2), and washed with brine (200 mL×2). The organic phase was dried with sodium sulfate, filtered, and concentrated to give the title compound as a brown solid (35 g, 66.9% yield). LCMS: rt=1.62 min, [M+H+]=267

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-9cbcd44b53eb424398e9a97c27f0bb8a
Source noteuspto-grants-2014_01