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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352638Generated: October 26, 2026

Hydrochloric Acid → Methyl 4-Boc-piperazine-2-acetate

https://huagongshe.com/reaction/352638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantMethyl 2-(1,4-dibenzylpiperazin-2-yl)acetateHCID 22710010—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 4-Boc-piperazine-2-acetateHCID 275681676.4%

Reaction Steps

The 13.7 g (40 mmol) of methyl 1,4-dibenzylpiperazine-2-acetate, 150 mL of MeOH, 50 mL of 1 N HCl (aqueous) and 3 g of 10% Pd/C were combined and hydrogenated with H2 (50 psi) for 24 hours. The reaction was filtered, the filtrate was concentrated in vacuo to remove most of the MeOH, and the residue was made basic with K2CO3 to pH=9-10, and 9.8 g (40 mmol) of BOC-ON was added slowly at 0° C. The reaction was stirred at 0° for 1 hour, allowed to warm up to room temperature, stirred for 2 hours, and extracted with ethyl acetate (2×200 mL). The combined extracts were treated with 50 mL of 10% HCl (aqueous). The aqueous layer was washed with ethyl acetate, basified with K2CO3 and extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo to give 7.89 g of methyl 4-Boc-piperazine-2-acetate; 1H NMR (CDCl3) δ1.4 (s, 9), 2.31 (dd, 1), 2.37 (dd, 1), 2.55 (b, 1), 2.69-3.02 (m, 4), 3.75 (s, 3), 3.88 (b, 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747031B2
Source datasetuspto-grants-2004_06
ORD IDord-8f01d00ff6df43a2bbeac16e7805914d
Source noteuspto-grants-2004_06