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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684770Generated: November 2, 2026

Water → 1-(Benzyloxycarbonyl)-4-phenylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/1684770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactant4-Piperidinecarboxylic acid, 4-phenyl-, 4-methylbenzenesulfonate (1:1)HCID 2723657—
SolventAcetoneHCID 180—
Product1-(Benzyloxycarbonyl)-4-phenylpiperidine-4-carboxylic acidHCID 2274179890.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 37.7 g of 4-carboxy-4-phenylpiperidine p-toluenesulfonate, 53.3 g of 30% aqueous NaOH solution and 250 ml of water is cooled to 5° C. A solution of 18 g of benzyl chloroformate in 60 ml of acetone is added rapidly at 5° C. and the reaction mixture is stirred overnight while the temperature is allowed to rise to RT. It is washed twice with ether and, after decantation, the aqueous phase is acidified to pH 1 by the addition of concentrated HCl and then 2N HCl. The precipitate formed is wrung, dried, taken up with ether and wrung again to give 30.6 g of the expected product. M.p.=142°-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05641777
Source datasetuspto-grants-1997_06
ORD IDord-aebe3c6fba1349c88b42d40d57d6127b
Source noteuspto-grants-1997_06