HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54551Generated: October 29, 2026
Sodium Hydroxide → 2-[1-(3-Methoxybenzyl)piperidin-4-yl]ethylamine
https://huagongshe.com/reaction/54551
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 2-[1-(3-Methoxybenzoyl)piperidin-4-yl]ethylamine | HCID 19959147 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-[1-(3-Methoxybenzyl)piperidin-4-yl]ethylamine | HCID 19959190 | 42.3% |
Reaction Steps
A solution of 2-[1-(3-methoxybenzoyl)piperidin-4-yl]ethylamine (4.5 g) in tetrahydrofuran (40 ml) was added dropwise to a suspension of lithium aluminum hydride (1.63 g) in tetrahydrofuran (50 ml) under refluxing. After 30 minutes, the mixture was cooled to 0° C., and ethyl acetate (5 ml), water (2 ml), 4N sodium hydroxide (4 ml), water (2 ml) and magnesium sulfate were added thereto successively. The resulting precipitates were removed out by filtration and the filtrate was evaporated in vacuo. The residue was chromagographed on alumina eluting with 2% methanol in chloroform to give 2-[1-(3-methoxybenzyl)piperidin-4-yl]ethylamine (1.8 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05622976 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-3fab7586478c4e548ab79ab1c26365a4 |
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| Source note | uspto-grants-1997_04 |
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