HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969643Generated: October 29, 2026
Acetic Acid → Ethyl 1-methylpiperidine-4-carboxylate
https://huagongshe.com/reaction/969643
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 1-methylpiperidine-4-carboxylate | HCID 11062856 | — |
Reaction Steps
Piperidine-4-carboxylic acid ethyl ester (78 g) was dissolved in MeOH (1.2 L) at RT then formaldehyde (37%, 90 mL) and acetic acid (42 mL) were added and stirred for 2 h. The mixture was cooled to 0° C., NaCNBH3 (70 g) was added, and the mix was stirred for 20 min at 0° C., then overnight at RT. The mixture was cooled to 0° C. then quenched with 6N NaOH. The mixture was concentrated in vacuo to an aqueous layer, which was extracted with EtOAc (4×), brine-washed, dried over Na2SO4, and concentrated in vacuo to provide 1-methylpiperidine-4-carboxylic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07307088B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-a3f11cbbf9eb41f584bea33b94c47dda |
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| Source note | uspto-grants-2007_12 |
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