HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856089Generated: October 29, 2026
p-Bromochlorobenzene → HCID 69479698, compound
https://huagongshe.com/reaction/856089
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-N-Boc-4-N-Methyl-aminopiperidine | HCID 2756806 | — |
| 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 | HCID 69479698 | HCID 69479698 | 134% |
Reaction Steps
A mixture of p-bromochlorobenzene (3.13 g, 16.3 mmol), tert-butyl (piperidin-4-yl)-N-methylcarbamate (3.5 g, 10.8 mmol), palladium acetate (73 mg, 0.33 mmol), (S)-(−)-BINAP (305 mg, 0.49 mmol) and sodium tert-butoxide (2.2 g, 22.9 mmol) in toluene (30 ml) was refluxed under a nitrogen atmosphere for 3 hours. Ethyl acetate and water were added to the reaction mixture, the mixture was stirred for a while. The insoluble substances were removed by filtration through Celite, and the filtrate was 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/ethyl acetate=10/1) to afford tert-butyl N-[1-(4-chlorophenyl)piperidin-4-yl]-N-methylcarbamate (4.7 g, yield 89%) 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-36264ef40ae2453896476c14795d283e |
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| Source note | uspto-grants-2007_08 |
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