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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526688Generated: October 27, 2026

Propanoic acid, 2-bromo-2-methyl-, ethyl ester → HCID 89907301, compound

https://huagongshe.com/reaction/526688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
ReactantSodium hydrideHCID 24758—
Reactant[5-(2,4-Dichloro-phenyl)-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-methanolHCID 89907741—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 89907301HCID 89907301—

Reaction Steps

To a solution of 500 mg of [5-(2,4-Dichloro-phenyl)-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-methanol in 6 ml of DMF were added 242 mg of sodium hydride (60% in mineral oil) at room temperature. After 15 min, 448 mg of tetrabutylammonium iodide and 946 mg of 2-Bromo-2-methyl-propionic acid ethyl ester were added and the reaction mixture was stirred for 16 h at room temperature. After dilution with saturated aqueous sodium hydrogen carbonate solution the reaction mixture was filtered through a chem Elut® cartridge by eluting with ethyl acetate The solvents were removed under reduced pressure and the crude product was purified by chromatography on silica gel eluting with a gradient of n-heptane/ethyl acetate. The fractions containing the product were combined and the solvent evaporated under reduced pressure. Yield: 200 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346757B2
Source datasetuspto-grants-2016_05
ORD IDord-5faf061e990b4b6fbe876e69eebfe214
Source noteuspto-grants-2016_05