HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734569Generated: October 30, 2026
Water → 4-amino-1-methyl-4-Piperidinemethanol
https://huagongshe.com/reaction/1734569
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Amino-1-methylpiperidine-4-carboxylic acid | HCID 272954 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-amino-1-methyl-4-Piperidinemethanol | HCID 15291735 | 98.9% |
Reaction Steps
Lithium aluminum hydride powder (15.62 g., 0.412 mole) in dry tetrahydrofuran (THF) (600 ml.) was heated under reflux for 15 minutes, after which 4-amino-1-methylpiperidine-4-carboxylic acid (31.0 g., 0.196 mole) in the form of a dry powder was added portionwise under nitrogen, with efficient stirring. After the addition was completed, the reaction mixture was heated under reflux for four hours, cooled to 0° C. under nitrogen with efficient stirring, worked up by careful slow addition of water (20 ml.), 15% aqueous NaOH (20 ml.) and again water (10 ml.). The reaction mixture was filtered and the precipitate was extracted with boiling THF (3 ×150 ml.). The THF liltrate and the extracts were combined and the solvent removed at 25 mm to give a yellow viscous oil (28.0 g., 98.9% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05534520 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-86056c785d4a4e1b8a867334cb8ef9a8 |
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| Source note | uspto-grants-1996_07 |
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