HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490329Generated: October 30, 2026
4-Bromobenzyl bromide → 1-[(4-Bromophenyl)methyl]piperidin-4-amine
https://huagongshe.com/reaction/490329
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | 1-[(4-Bromophenyl)methyl]piperidin-4-amine | HCID 23312456 | 87.8% |
Reaction Steps
To a solution of 4-bromo benzylbromide (1.0 g, 4.1 mmol) in dichloromethane (20 ml) and diisopropyletylamine (1 ml) was added tert-butyl 4-piperidinylcarbamate (1.0 g, 5.0 mmol). The solution was then stirred at room temperature over night. The solvent was evaporated and 25 ml of 50% TFA in dichloromethane was added to the resulting white solid. The mixture was then stirred at room temperature for 2 h and then evaporated to dryness. The resulting solid was dissolved in water and extracted with toluene. After removal of the toluene the water phase was made basic with 1M NaOH giving a pH of 13. The water phase was then extracted with dichloromethane 3 times and the combined extracts were dried and then evaporated to give the pure product as a slightly yellow oil (0.96 g, 3.6 mmol)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528156B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-05781c454d734c16a82b7b62dcde2f08 |
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| Source note | uspto-grants-2009_05 |
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