HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371982Generated: October 31, 2026
tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(4-chloro-3-methoxyphenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1371982
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 5-Bromo-2-chloroanisole | HCID 2769567 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | Tert-butyl 4-(4-chloro-3-methoxyphenyl)piperazine-1-carboxylate | HCID 58778031 | — |
Reaction Steps
An oven dried glass vial was charged with 5-Bromo-2-chloroanisole (1.0 mmol), N-Bocpiperazine (1.2 mmol), NaOtBu (1.4 mmol), tris(dibenzylideneacetone)-dipalladium(0) {Pd2dba3} (0.0025 mmol, 0.5 mol %) and BINAP (0.0075 mmol), and the vial was then flushed with nitrogen and capped tightly. The mixture was heated to 80° C. overnight and then cooled to room temperature, taken up in ether, filtered and concentrated. The crude product was purified by flash column chromatography on silica gel with ethyl acetate to yield 4-(4-Chloro-3-methoxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157464B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-6f0e535e4c21451b891cd0548e635de3 |
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| Source note | uspto-grants-2007_01 |
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