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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406653Generated: November 1, 2026

Piperazine → 1-(4-tert-Butylbenzyl)piperazine

https://huagongshe.com/reaction/1406653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
SolventTetrahydrofuranHCID 8028—
Product1-(4-tert-Butylbenzyl)piperazineHCID 2735657—

Reaction Steps

Synthesized according to General Procedure A: 4-tert-butylbenzyl bromide (4{20}, 4.05 mL, 22.0 mmol, 1 equiv.), piperazine (11.4 g, 132.1 mmol, 6 equiv.), THF (48.1 mL). Purification with flash column chromatography on silica gel (4:1 EtOAc:MeOH) afforded 5{20} (3.75 g, 73%) as a beige solid. 1H-NMR (500 MHz, CDCl3): δ 7.30 (d, 2H, J=8.5 Hz), 7.22 (d, 2H, J=8.5 Hz), 3.44 (s, 2H), 2.85 (t, 4H, J=5.0 Hz), 2.38 (br s, 4H), 1.54 (br s, 1H), 1.29 (s, 9H). 13C-NMR (125 MHz, CDCl3): δ 149.6, 134.7, 128.7, 124.8, 63.1, 54.3, 45.9, 34.2, 31.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916705B2
Source datasetuspto-grants-2014_12
ORD IDord-61c80f69028b4082b38d04df64e0295e
Source noteuspto-grants-2014_12