HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16364Generated: October 25, 2026
Tetrahydrofuran → [(2R,6S)-6-(4-chlorophenyl)piperidin-2-yl]methanol
https://huagongshe.com/reaction/16364
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | methyl(2R,6S)-6-(4-chlorophenyl)piperidine-2-carboxylate | HCID 67462967 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [(2R,6S)-6-(4-chlorophenyl)piperidin-2-yl]methanol | HCID 67460196 | 86.5% |
Reaction Steps
In nitrogen atmosphere, (2R,6S)-6-(4-chlorophenyl)piperidine-2-carboxylic acid methyl ester (2.47 g) was added to a THF suspension (50 mL) of lithium aluminium hydride (508 mg) at −20° C. The resulting reaction solution was stirred at −20° C. for 1 hr, and then water (0.51 mL), a 5 N sodium hydroxide aqueous solution (0.51 mL), and water (1.53 mL) were added thereto in this order at −20° C. The resulting reaction solution was stirred at room temperature for 15 min, and then ethyl acetate was added thereto. The resulting 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, eluting solvent: heptane-ethyl acetate system) to give 1.90 g of the title compound. The physical property values of this compound were as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737141B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-215bc8314c444776914eedc2a913ef7b |
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| Source note | uspto-grants-2010_06 |
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