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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1-isopropylpiperidine-4-carboxylateHCID 19900430—
SolventEthanolHCID 702—
Product1-Isopropylpiperidine-4-Carboxylic AcidHCID 648418799.3%

Reaction Conditions

Temperature34 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129245B2
Source datasetuspto-grants-2006_10
ORD IDord-97eadcb6ab32438586ddd480aab1b733
Source noteuspto-grants-2006_10