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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526703Generated: October 27, 2026

Propanoic acid, 2-bromo-2-methyl-, ethyl ester → HCID 89907577, compound

https://huagongshe.com/reaction/526703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
ReactantSodium hydrideHCID 24758—
Reactant[1-(2,4-Dichloro-phenyl)-4-methyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazol-3-yl]-methanolHCID 89907507—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 89907577HCID 89907577—

Reaction Steps

To a solution of 2 g of [1-(2,4-Dichloro-phenyl)-4-methyl-5-(4-trifluoromethyl-phenyl)-1H-pyrazol-3-yl]-methanol in 15 ml of DMF were added 997 mg of sodium hydride (60% in mineral oil) at room temperature. After 15 min 1.8 g of tetrabutylammonium iodide and 2.9 g 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: 1.3 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346762B2
Source datasetuspto-grants-2016_05
ORD IDord-e03e763485fe4deaa5af0708476c9b2a
Source noteuspto-grants-2016_05