HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428045Generated: October 29, 2026
N-bromobutanimide → 1-[4-(4-Amino-3-bromo-phenyl)-piperidin-1-yl]-ethanone
https://huagongshe.com/reaction/1428045
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-[4-(4-Aminophenyl)piperidin-1-yl]ethanone | HCID 59128551 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[4-(4-Amino-3-bromo-phenyl)-piperidin-1-yl]-ethanone | HCID 59128592 | — |
Reaction Steps
A solution of 1-[4-(4-amino-phenyl)-piperidin-1-yl]-ethanone (as prepared in the previous step, 0.36 g, 1.66 mmol) in CH2Cl2 (10 mL) was cooled to −78° C. and treated with NBS (0.28 g, 1.58 mmol) as a suspension in CH2Cl2 (4 mL). The reaction was allowed to warm to room temperature and stir for 30 min. The reaction was diluted with CH2Cl2 and washed with saturated aqueous NaHCO3. The organic layer was dried over MgSO4 and concentrated in vacuo. The crude material was used directly in the next reaction. LC-MS (ESI, m/z): Calcd. for C13H17BrN2O 297.1 (M+H). found 297.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933091B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-6edce4c159f8464cb5ddebdfffc887f3 |
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| Source note | uspto-grants-2015_01 |
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