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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371006Generated: October 30, 2026

Ethyl Acetate → HCID 86062444, compound

https://huagongshe.com/reaction/2371006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1,1,1,3,3,3-Hexafluoro-2-propanolHCID 13529—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-4-methyl-5-nitropyridineHCID 345364—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86062444HCID 8606244485.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

After 1.33 g of 60% sodium hydride was introduced to 15 ml of tetrahydrofuran and cooled to 5° C., 5.84 g of 1,1,1,3,3,3-hexafluoro-2-propanol was added dropwise. The mixture was stirred at 5° C. for 30 minutes, and then 3.0 g of 2-chloro-4-methyl-5-nitropyridine dissolved in 10 ml of tetrahydrofuran was added dropwise, this being stirred at room temperature for 3 hours. After being left at room temperature for 3 days, ethyl acetate and water were added thereto, and the organic layer was separated and washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=10:1) to give 4.5 g (yield 80%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710234B2
Source datasetuspto-grants-2014_04
ORD IDord-517730e03bd54e2dbf2de4bf370f5f20
Source noteuspto-grants-2014_04