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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355464Generated: October 26, 2026

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

https://huagongshe.com/reaction/355464

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-toluenesulphonate, 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 mixture is left stirring overnight while allowing the temperature to rise to RT. The reaction mixture is washed twice with ether and, after settling has taken place, the aqueous phase is separated and acidified to pH 1 by adding concentrated HCl and then 2N HCl. The precipitate formed is drained, dried, taken up in ether and drained again. 30.6 g of the expected product are obtained, m.p.=142°-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05830906
Source datasetuspto-grants-1998_11
ORD IDord-9edd3216b4c04336a113c215dc3d42bf
Source noteuspto-grants-1998_11