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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598449Generated: November 2, 2026

4-Benzyl-1-tert-butoxycarbonyl-2(S)-(2-methoxyethyl)piperazine → (S)-Tert-butyl 2-(2-methoxyethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1598449

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyl-1-tert-butoxycarbonyl-2(S)-(2-methoxyethyl)piperazineHCID 15406046—
CatalystPalladiumHCID 23938—
Product(S)-Tert-butyl 2-(2-methoxyethyl)piperazine-1-carboxylateHCID 15406047—

Reaction Steps

The title compound was prepared according to the procedure described in Example 2, Step C, except using 4-benzyl-1-tert-butoxycarbonyl-2(S)-(2-methoxyethyl)piperazine (0.280 g, 0.83 mmol) and 10% palladium on carbon (80 mg). The title compound was obtained as an oil (179 mg). NMR (CD3OD, 300 MHz) δ 4.17 (1H, m), 3.81 (1H, dd, J=3, 13 Hz), 3.38 (2H, t, J=6 Hz), 2.82-3.02 (2H, m), 2.77 (2H, ABq, J=4, 13 Hz), 2.59 (1H, dt, J=4, 7 Hz), 2.04 (1H, m), 1.84 (1H, m), 1.46 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736539
Source datasetuspto-grants-1998_04
ORD IDord-c1d9a9bdfe8d42d9b633ec544cf0328a
Source noteuspto-grants-1998_04