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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71775Generated: October 25, 2026

4-Piperidinecarboxylic acid → 1-Carbobenzoxy-4-piperidinecarboxylic Acid

https://huagongshe.com/reaction/71775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidinecarboxylic acidHCID 3773—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
Product1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 73648991.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Piperidine-4-carboxylic acid (64.8 g, 0.5 mol) in H2O (50 mL) was treated with NaOH (44.0 g, 1.1 mol). The reaction mixture was cooled to 0° C. and treated with CbzCl (93.8 g, 0.55 mol). The reaction mixture was stirred at ambient temperature for 4 hours and the mixture was extracted with Et2O (3 150 mL). The aqueous phase was acidified with 6 N HCl (140 mL) and extracted with EtOAc (3 200 mL). The solution was dried over MgSO4, filtered, and concentrated to afford crude piperidine-1,4-dicarboxylic acid monobenzyl ester (120 g), which was used without further purification: MS (ESI) m/z 262 [M−H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822430B2
Source datasetuspto-grants-2014_09
ORD IDord-faee25c567534f6e93cd002eea407fee
Source noteuspto-grants-2014_09