HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270997Generated: October 31, 2026
HCID 11128927, compound → HCID 10967168, compound
https://huagongshe.com/reaction/2270997
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11128927 | HCID 11128927 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | HCID 178418361 | HCID 178418361 | — |
| Product | HCID 10967168 | HCID 10967168 | 90.3% |
Reaction Steps
A solution of ethyl 1-tert-butoxycarbonyl-1,4,5,6-tetrahydropyrazine-2-carboxylate (69.0 g) in acetic acid (AcOH, 500 ml) was subjected to catalytic reduction using platinum dioxide (4.0 g) at 40° C. in hydrogen at 3 atm for 4 hours. The catalyst was removed by filtration, and the filtrate was concentrated in vacuo. The residue was dissolved in H2O (800 ml) and the solution was washed with Et2O (500 ml×2). To the aqueous layer was added NaHCO3 to adjust the pH of the solution to 8 and the solution was extracted with AcOEt (800 ml×2). The combined organic layer was washed with saturated aqueous NaHCO3 solution and brine, dried over MgSO4 and concentrated in vacuo to give 62.8 g of ethyl 1-tert-butoxycarbonyl- piperazine-2-carboxylate as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06333324B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-8da586f7399748e0ba73f6af641a2963 |
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| Source note | uspto-grants-2001_12 |
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