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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625196Generated: October 31, 2026

Cesium carbonate → Methyl 4-tert-butyl-2-(6-(trifluoromethyl)pyridin-2-yloxy)benzoate

https://huagongshe.com/reaction/1625196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant2-Fluoro-6-(trifluoromethyl)pyridineHCID 2736501—
ReactantMethyl 4-tert-butyl-2-hydroxybenzoateHCID 20777194—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-tert-butyl-2-(6-(trifluoromethyl)pyridin-2-yloxy)benzoateHCID 5768771141%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of methyl 4-tert-butyl-2-hydroxybenzoate (0.70 g, 3.4 mmol), 2-fluoro-6-(trifluoromethyl)pyridine (0.55 g, 3.4 mmol), and Cs2CO3 (1.1 g, 3.4 mmol) in DMF (15 mL) was heated at 70° C. for 19 hours. The reaction was diluted with water and extracted with ethyl acetate. The combined extracts were washed with brine and water, dried over sodium sulfate, and evaporated. The residue was purified by column chromatography on silica gel with 0-15% ethyl acetate in hexanes to give methyl 4-tert-butyl-2-(6-(trifluoromethyl)pyridin-2-yloxy)benzoate (0.49 g, 41% yield). LC/MS: m/z 354.3 (M+H)+ at 2.13 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779197B2
Source datasetuspto-grants-2014_07
ORD IDord-6cf6dc06926e4194baff3ed4f64a4d49
Source noteuspto-grants-2014_07