HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247041Generated: October 30, 2026
Hydrochloric Acid → 1-Isopropylpiperidine-4-Carboxylic Acid
https://huagongshe.com/reaction/1247041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 1-isopropylpiperidine-4-carboxylate | HCID 19900430 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Isopropylpiperidine-4-Carboxylic Acid | HCID 6484187 | 99.3% |
Reaction Steps
Crude ethyl 1-isopropylpiperidine-4-carboxylate (63.39 g, 318.0 mmol) was dissolved in ethanol (500 mL), and NaOH (25.3 g, 632 mmol) was added. The solution was heated to reflux for 15.75 h at which point it was allowed to cool to 34° C. A solution of ethanolic HCl (220 mL, 2.9 M solution) was added rapidly which caused a mild exotherm and immediate precipitation. The resulting NaCl was filtered using a fritted funnel, and the cloudy filtrate was refiltered through diatomaceous earth. The filtrate was concentrated and dissolved in 50% EtOAc/EtOH (600 mL) and heated on a steam bath. The insoluble material was removed by a filtration through diatomaceous earth, and the resulting filtrate was concentrated to a solid which was dried in a 50° C. vacuum oven to yield 54.09 g of yellow solid (corrected for 0.2 wt % EtOH by 1H-NMR analysis) which is a 99% yield over two steps. No further purification was attempted:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07129245B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-97eadcb6ab32438586ddd480aab1b733 |
|---|
| Source note | uspto-grants-2006_10 |
|---|