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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453907Generated: October 30, 2026

Water → 1-Carbobenzoxy-4-piperidinecarboxylic Acid

https://huagongshe.com/reaction/453907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Piperidinecarboxylic acidHCID 3773—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
Product1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 736489—

Reaction Conditions

Temperature0 °C

Reaction Steps

To piperidine-4-carboxylic acid (25 g) in THF (75 ml) there was added water (75 ml), followed by sodium bicarbonate (30.8 g). The mixture was cooled to 0° C., and Cbz chloride (38.9 ml) was added dropwise. The reaction mixture was then stirred for 5 h at room temperature (TLC monitoring). When the reaction was complete, the organic solvent was distilled off and the residue was taken up in water (200 ml) and washed with ethyl acetate (2×150 ml). The aqueous phase was acidified with dilute aqueous HCl solution and extracted with ethyl acetate. The organic phase was dried (Na2SO4) and concentrated under vacuum. Yield: 48.5 g (96%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492559B2
Source datasetuspto-grants-2013_07
ORD IDord-cad9ed4859e34008ad4bfb60f139c827
Source noteuspto-grants-2013_07