HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727211Generated: October 31, 2026
(3-Bromopropyl)benzene → 1-[4-(3-Phenylpropoxy)-1-piperidinyl]ethanone
https://huagongshe.com/reaction/1727211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Hydroxypiperidin-1-yl)ethan-1-one | HCID 10749291 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[4-(3-Phenylpropoxy)-1-piperidinyl]ethanone | HCID 69054323 | 27.4% |
Reaction Steps
1-Acetylpiperidin-4-ol (Preparation 193, 8 g, 60 mmol) in N,N-dimethylformamide (50 ml) was added dropwise to a stirred suspension of sodium hydride (50% wt dispersion in oil, 3.68 g, 80 mmol) in N,N-dimethylformamide (50 ml) at room temperature under nitrogen. After stirring the reaction mixture for 4 hours, 1-bromo-3-phenylpropane (12.94 g, 65 mmol) in N,N-dimethylformamide (50 ml) was added dropwise to the solution at 0° C. and the reaction mixture was stirred for a further 4 h. The solution was diluted with isopropyl alcohol (20 ml) and water (100 ml) and then evaporated to give a semi solid. Water (100 ml) was added and the solution was extracted with petroleum ether (3×100 ml). The combined organic extracts were dried (Na2SO4) and concentrated in vacuo to give an orange oil (4.3 g, 27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07494992B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-1d4a94d44e824426a692d6139dca7bda |
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| Source note | uspto-grants-2009_02 |
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