HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856072Generated: October 27, 2026
p-Bromochlorobenzene → Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate
https://huagongshe.com/reaction/856072
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate | HCID 1491503 | 86% |
Reaction Steps
A mixture of p-bromochlorobenzene (1.91 g, 9.99 mmol), tert-butyl 4-aminopiperidine-1-carboxylate (2.0 g, 9.99 mmol), palladium acetate (45 mg, 0.2 mmol), (R)-(+)-BINAP (187 mg, 0.3 mmol) and sodium tert-butoxide (1.35 g, 14.0 mmol) in toluene (20 ml) was refluxed under a nitrogen atmosphere for 1 hour. Ethyl acetate and water were added to the reaction mixture while stirring, the insoluble substances were removed by filtration through Celite, and the filtrate was then extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (methylene chloride/methanol=100/1) to afford tert-butyl 4-(4-chlorophenylamino)piperidine-1-carboxylate (2.67 g, yield 86%) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262212B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-c276d8dff44d4683981ae2411bdadb15 |
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| Source note | uspto-grants-2007_08 |
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