HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727209Generated: November 2, 2026
Water → 1-Acetyl-4-{[(4-chlorophenyl)methyl]oxy}piperidine
https://huagongshe.com/reaction/1727209
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Hydroxypiperidin-1-yl)ethan-1-one | HCID 10749291 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Acetyl-4-{[(4-chlorophenyl)methyl]oxy}piperidine | HCID 69056298 | 84.3% |
Reaction Steps
1-Acetylpiperidin-4-ol (Preparation 193, 10 g, 70 mmol) in N,N-dimethylformamide (50 ml) was added dropwise to a stirred suspension of sodium hydride (50% wt dispersion in oil, 4.8 g, 0.1 mol) in N,N-dimethylformamide (50 ml) at room temperature under nitrogen. After stirring the reaction mixture for 3 hours, 4-chlorobenzyl chloride (12.8 g, 80 mmol) in N,N-dimethylformamide (50 ml) was added dropwise and the reaction mixture was stirred for a further 4 h. The solution was filtered and the filtrate was evaporated to give an orange oil. Water was added and the mixture was extracted with petroleum ether (3×50 ml) and then with diethyl ether (3×50 ml). The combined organic extracts were dried (Na2SO4) and concentrated to give the title compound as an orange oil (15.8 g, 84%).
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-e6a512af005746f9970888d411622068 |
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| Source note | uspto-grants-2009_02 |
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