HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278518Generated: November 3, 2026
Toluene → (-)-trans-4-(4'-Fluorophenyl)-3-hydroxymethyl-N-methylpiperidine
https://huagongshe.com/reaction/1278518
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | trans-3-Ethoxycarbonyl-4-(4'-fluorophenyl)-1-methylpiperidine-2,6-dione | HCID 15405466 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran toluene | HCID 22635083 | — |
| Product | (-)-trans-4-(4'-Fluorophenyl)-3-hydroxymethyl-N-methylpiperidine | HCID 2734218 | — |
Reaction Steps
To a cooled solution of LiAlH4 (0.22 mol) in toluene/THF under argon was added (+/−) trans-3-ethoxycarbonyl-4-(4′-fluorophenyl)-N-methyl-piperidine-2,6-dione (0.083 mol) in THF holding the temperature below 15° C. After addition was complete, the reaction was allowed to warm to room temperature. After 30 minutes at room temperature reaction was heated to >40° C. for 2 hr. Reaction was then cooled to <5° C. and toluene (50 ml) was added. Water (9 ml) was then added slowly holding the temperature below 15° C. Additional H2O or aqueous NaOH was used as necessary. The solid inorganic salts were removed by filtration. These solids were washed with additional THF or toluene. The filtered solution was then concentrated to give (+/−) trans-4-(4′-fluorophenyl)-3-hydroxymethyl-N-methylpiperidine in higher yield (but similar impurity profile) as with NaAlH4 as shown by HPLC analysis. The product can be recovered by standard procedures such as trituration with a less polar solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06444190B2 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-2aa132d7e98c4a0ea35b10fc28db711d |
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| Source note | uspto-grants-2002_09 |
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