HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405434Generated: November 2, 2026
1-Bromo-3-chlorobenzene → Tert-butyl 4-(3-chlorophenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1405434
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-chlorobenzene | HCID 7928 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 4-(3-chlorophenyl)piperazine-1-carboxylate | HCID 11087774 | 83.3% |
Reaction Steps
A solution of t-butyl piperazine-1-carboxylate (1.96 g, 10.54 mmol, 2.00 equiv), 1-bromo-3-chlorobenzene (1 g, 5.26 mmol, 1.00 equiv), BINAP (330 mg, 0.53 mmol, 0.10 equiv), Pd2(dba)3 (243.8 mg, 0.27 mmol, 0.05 equiv), NaOt-Bu (1.59 g, 16.56 mmol, 3.00 equiv), and toluene (17 mL) was placed in a 100-mL round bottom flask, stirred overnight at 100° C. in an oil bath, and concentrated under vacuum. Purification via silica gel column (PE/EA (50:1)) yielded 1.3 g (83%) of t-butyl 4-(3-chlorophenyl)piperazine-1-carboxylate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916560B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-79568a8f03a141b48201f2ac8bc70477 |
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| Source note | uspto-grants-2014_12 |
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