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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534942Generated: November 2, 2026

Water → Ethyl [4-(2-tert-butyl-4-methylphenyl)piperazin-1-yl](oxo)acetate

https://huagongshe.com/reaction/534942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantEthoxalyl chlorideHCID 20884—
Reactant1-(2-Tert-butyl-4-methylphenyl)piperazine dihydrochlorideHCID 66750837—
SolventTetrahydrofuranHCID 8028—
ProductEthyl [4-(2-tert-butyl-4-methylphenyl)piperazin-1-yl](oxo)acetateHCID 6675104671.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of 1-(2-tert-butyl-4-methylphenyl)piperazine dihydrochloride (Reference Example 10, 0.300 g, 0.98 mmol) and triethylamine (548 μl, 3.93 mmol) in THF (10 mL) stirring at 0° C. was added ethyl chloro(oxo)acetate (0.175 mg, 1.28 mmol). The mixture was warmed to room temperature. After 3 days the reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and the solvent was evaporated under reduced pressure to give the crude product. The product was purified by flash column chromatography (silica gel, n-hexane/ethyl acetate=90:10 to 50:50) to provide ethyl [4-(2-tert-butyl-4-methylphenyl)piperazin-1-yl](oxo)acetate (0.233 g, 71%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-b0458f87bee149ea80babd901f11aee1
Source noteuspto-grants-2014_10