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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186192Generated: October 31, 2026

Sodium hydride → Methyl 5-(2,2,2-trifluoroethoxy)pyridine-2-carboxylate

https://huagongshe.com/reaction/1186192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
ReactantMethyl 5-hydroxypyridine-2-carboxylateHCID 4715126—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-(2,2,2-trifluoroethoxy)pyridine-2-carboxylateHCID 5747587370.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-hydroxy-pyridine-2-carboxylic acid methyl ester (200 mg) in DMF (2.0 ml) was added at 22° C. NaH (55% in oil, 64 mg) and stirring was continued until gas evolution ceased. The suspension was cooled to 0° C. and treated with trifluoroethyl trifluormethane sulphonate (728 mg) and stirring was continued at 22° C. for 2 h. The mixture was partitioned between saturated NaHCO3 and ethyl acetate and the organic layer was dried and evaporated. The residue was purified by chromatography on silica using n-heptane/ethyl acetate (3:1) to give 5-(2,2,2-trifluoro-ethoxy)-pyridine-2-carboxylic acid methyl ester (216 mg) as a white solid. MS (ISP): m/z=236.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673894B2
Source datasetuspto-grants-2014_03
ORD IDord-ab9277e42f1c4422a7183475775bdfce
Source noteuspto-grants-2014_03