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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598446Generated: November 3, 2026

(S)-tert-Butyl 2,4-dibenzylpiperazine-1-carboxylate → 1,1-Dimethylethyl (2S)-2-(phenylmethyl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/1598446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-tert-Butyl 2,4-dibenzylpiperazine-1-carboxylateHCID 22884141—
CatalystPalladiumHCID 23938—
Product1,1-Dimethylethyl (2S)-2-(phenylmethyl)-1-piperazinecarboxylateHCID 17750441—

Reaction Steps

The title compound was prepared according to the procedure described in Example 2, Step C, except using 1-tert-butoxycarbonyl-2(S),4-dibenzylpiperazine (4.78 g, 11.3 mmol) and 10% palladium on carbon (1.04 g). The title compound was obtained as an oil. NMR (300 MHz, CD3OD) δ 7.25 (5H, m), 4.35 (1H, m), 4.00 (1H, d, J=12 Hz), 2.7-3.3 (7H, m), 1.25 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736539
Source datasetuspto-grants-1998_04
ORD IDord-72949014fd5c48669a27eb5d4127551f
Source noteuspto-grants-1998_04