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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | 1-(2-Tert-butyl-4-methylphenyl)piperazine dihydrochloride | HCID 66750837 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl [4-(2-tert-butyl-4-methylphenyl)piperazin-1-yl](oxo)acetate | HCID 66751046 | 71.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853215B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-b0458f87bee149ea80babd901f11aee1 |
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| Source note | uspto-grants-2014_10 |
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