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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557004Generated: October 29, 2026

p-Bromochlorobenzene → 4-(4-Chloro-phenyl)-3-methyl-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/557004

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
ReactantBinap, (A+-)-HCID 634876—
Reactanttert-Butyl 3-methylpiperazine-1-carboxylateHCID 2756810—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) dibenzylideneacetoneHCID 86611386—
Product4-(4-Chloro-phenyl)-3-methyl-piperazine-1-carboxylic acid tert-butyl esterHCID 6675795768%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 3-Methyl-piperazine-1-carboxylic acid tert-butyl ester (1.0 g, 5 mmol) and 4-bromochlorobenzene (0.77 g, 4 mmol) was added sodium tert-butoxide (0.96 g, 10 mmol), palladium(II) dibenzylideneacetone (Pd2DBA3, 0.09 g, 0.1 mmol), and BINAP (0.19 g, 0.3 mmol). The suspension was stirred at 120° C. for 10 hours. The reaction was filtered through celite and evaporated in vacuo. The residue was purified by silica gel chromatography (hexane-ethyl acetate) to yield 0.84 g (68%) of the title compound. 1H-NMR (CDCl3): δ 1.00 (3H, m), 1.74 (9H, s), 3.10 (3H, m), 3.30 (1H, m), 3.80 (2H, m), 4.10 (1H, brs), 6.85 (2H, d), 7.20 (2H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058287B2
Source datasetuspto-grants-2011_11
ORD IDord-ad87eb8aa4cd460a8e49301a95a261ca
Source noteuspto-grants-2011_11