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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355700Generated: October 31, 2026

Acetic Acid → HCID 53730400, compound

https://huagongshe.com/reaction/355700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiethyl OxalateHCID 7268—
ReactantHCID 21714329HCID 21714329—
ReactantPotassium ethoxideHCID 23670592—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53730400HCID 53730400—

Reaction Steps

Diethyl oxalate (1.94 g, 13.2 mmol) and then a solution of 2-methyl-4-[N-methyl-N-[2-(2-tetrahydro-2H-pyranyl) oxyethyl]amino]-3-nitrobenzotrifluoride (2.40 g, 6.62 mmol) in tetrahydrofuran (40 ml) were added dropwise to a mixture of potassium ethoxide (1.11 g, 13.2 mmol) and tetrahydrofuran (60 ml) at room temperature. The reaction mixture was stirred at room temperature for 6 hours and then cooled to 3° C., and acetic acid (1.59 g, 26.5 mmol) was added dropwise. The reaction mixture thus obtained was poured into cold water and extracted twice with ethyl acetate. The extract solution was washed with a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate/n-hexane= 1/9) to obtain an oil of ethyl [3-[N-methyl-N-[2-(2-tetrahydro-2H-pyranyl)oxyethyl]-amino]-2-nitro-6-trifluoromethylphenyl]pyruvate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834454
Source datasetuspto-grants-1998_11
ORD IDord-e8fe0b56d2294ddf9f0d1e0e56f40c5e
Source noteuspto-grants-1998_11