HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642813Generated: October 29, 2026
Dimethylformamide → Ethyl 5-(4-ethylphenyl)1-[(4-hydroxypiperidin-1-yl)carbonyl]piperidine-3-carboxylate
https://huagongshe.com/reaction/1642813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | 3-Ethyl 1-(4-nitrophenyl) 5-(4-ethylphenyl)piperidine-1,3-dicarboxylate | HCID 58002474 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 5-(4-ethylphenyl)1-[(4-hydroxypiperidin-1-yl)carbonyl]piperidine-3-carboxylate | HCID 58002667 | — |
Reaction Steps
370 mg (0.81 mmol) of 3-ethyl 1-(4-nitrophenyl) 5-(4-ethylphenyl)piperidine-1,3-dicarboxylate, 245 mg (2.42 mmol) of 4-hydroxypiperidine and 112 mg (0.81 mmol) of potassium carbonate were added to 9 ml of DMF and heated in a single-mode microwave (Emrys Optimizer) at 150° C. for 15 min. For work-up, water was added and the reaction solution was extracted with ethyl acetate. The organic phase was dried with sodium sulphate and concentrated under reduced pressure. The residue was purified by preparative HPLC. Yield: 208 mg (66% of theory)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119663B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-8f0ae3ddae6f4931bb418d4dde41c6d3 |
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| Source note | uspto-grants-2012_02 |
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