HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10784Generated: October 26, 2026
Triethylamine → 2-Bromo-1-(4-(piperidin-1-yl)phenyl)ethanone
https://huagongshe.com/reaction/10784
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethylphosphite | HCID 3780918 | — |
| Reactant | 2,2-Dibromo-1-[4-(1-piperidinyl)phenyl]ethanone | HCID 14373045 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-1-(4-(piperidin-1-yl)phenyl)ethanone | HCID 15864546 | 100% |
Reaction Steps
2,2-Dibromo-1-[4-(1-piperidinyl)phenyl]ethanone (3 g, 8.3 mmol) (from Step A above) was dissolved in tetrahydrofuran (15 mL), and cooled to 0° C. To the resulting solution were added dropwise diethylphosphite (1.13 mL, 8.7 mmol) and triethylamine (1.21 mL, 8.7 mmol) in tetrahydrofuran (7 mL) at 0° C. with stirring. The mixture was slowly warmed to room temperature and stirred for 6 h. The reaction mixture was concentrated in vacuo and poured into ice/water. The precipitate was collected by filtration, washed with water and dried in vacuo to provide 2-bromo-1-[4-(1-piperidinyl)phenyl]ethanone (2.3 g, 100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094896B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-ff4256aaf0c04c6c9ceb8c97dc41cecd |
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| Source note | uspto-grants-2006_08 |
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