HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212180Generated: October 26, 2026
Acetic Acid → Methyl 3-aminopiperidine-1-carboxylate
https://huagongshe.com/reaction/2212180
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-(Trityl-amino)-piperidine-1-carboxylic acid methyl ester | HCID 69652409 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 3-aminopiperidine-1-carboxylate | HCID 22273098 | 95.6% |
Reaction Steps
Add acetic acid saturated with HCl(g) (100 mL, ˜3N in HCl) to 3-(trityl-amino)-piperidine-1-carboxylic acid methyl ester (6.51 g, 16.2 mmol). Stir the solution vigorously at room temperature for 2 hours. Concentrate the reaction, follow this by addition of acetonitrile and concentration to assist in the removal of acetic acid (×2). Partition the resulting material between 1N HCl and ethyl acetate, separate the layers, extract the organic layer with 1N HCl. Basify the combined aqueous layers with 5N sodium hydroxide, extract with 20% isopropanol/chloroform (×3). Dry the combined organic layers over magnesium sulfate and concentrate to give 2.45 g of the title compound as a white solid, 95% yield. 1H NMR: consistent with structure. MS (ion spray) 158 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101891B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-8d411f7d4713493f87e38178998d2b8d |
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| Source note | uspto-grants-2006_09 |
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