HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436156Generated: October 25, 2026
Water → [(2R,6S)-6-(4-chlorophenyl)piperidin-2-yl]methanol
https://huagongshe.com/reaction/1436156
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | methyl(2R,6S)-6-(4-chlorophenyl)piperidine-2-carboxylate | HCID 67462967 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [(2R,6S)-6-(4-chlorophenyl)piperidin-2-yl]methanol | HCID 67460196 | 86.5% |
Reaction Steps
Lithium aluminum hydride (508 mg) was suspended in THF (50 mL) in a nitrogen atmosphere. Methyl (2R,6S)-6-(4-chlorophenyl)piperidine-2-carboxylate (2.47 g) was added to the suspension at −20° C., and the reaction solution was stirred at −20° C. for one hour. Water (0.51 ml), a 5 N sodium hydroxide solution (0.51 ml), and water (1.53 ml) were sequentially added to the reaction solution at −20° C., and the reaction solution was stirred at room temperature for 15 minutes. Ethyl acetate was added to the reaction solution. Then, the reaction solution was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (carrier: Chromatorex NH; elution solvent: heptane-ethyl acetate system) to obtain 1.90 g of the title compound. The property value of the compound is as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618960B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-3cdcfb92dc344b60b25eb750a4f762c8 |
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| Source note | uspto-grants-2009_11 |
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