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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271006Generated: November 1, 2026

Water → HCID 10967168, compound

https://huagongshe.com/reaction/2271006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 11128927HCID 11128927—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventHCID 178418361HCID 178418361—
ProductHCID 10967168HCID 1096716897.9%

Reaction Steps

Ethyl 1-tert-butoxycarbonyl-1,4,5,6-tetrahydropyrazinecarboxylate (60 g) was dissolved in AcOH (400 ml), and the solution was subjected to catalytic reduction using 10% palladium on carbon (12 g)-H2O (30 ml), in hydrogen at 3 atm for 4 hours. The catalyst was removed by filtration and the filtrate was concentrated under reduced pressure. The residue was dissolved in AcOEt (1000 ml), and the organic layer was washed with saturated aqueous NaHCO3 solution by stirring carefully to avoid foaming. The organic layer was further washed with saturated brine, and dried over anhydrous MgSO4. The solvent was evaporated under reduced pressure to give 59.2 g of ethyl 1-tert-butoxycarbonyl-2-piperazinecarboxylate as an oil (yield 97.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333324B1
Source datasetuspto-grants-2001_12
ORD IDord-5f169860b3774c89be48eb146a9f3d47
Source noteuspto-grants-2001_12