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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849334Generated: October 30, 2026

4-Piperidinecarboxylic acid, 4-phenyl-, 4-methylbenzenesulfonate (1:1) → 1-Benzyl-4-phenylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/849334

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidinecarboxylic acid, 4-phenyl-, 4-methylbenzenesulfonate (1:1)HCID 2723657—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product1-Benzyl-4-phenylpiperidine-4-carboxylic acidHCID 9657689.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

106 ml of a 30 % NAOH solution is added to a suspension of 100 g of 4-carboxy-4-phenylpiperidine p-toluenesulfonate in 600 ml of water, then the thus obtained solution is cooled to 5° C., a solution of 47.6 g of bromide benzyl in 100 ml of acetone is added dropwise and left under stirring for 1 hour while the temperature being allowed to rise to RiT. The acetone is evaporated under vacum, and the pH of the remaining aqueous phase is brought to 9.5 by adding concentrated aqueous solution of HCl, then the pH is adjusted to 8.5 by adding a 2N HCl solution. The precipitate formed is wrung and washed with water and then with acetone to give 70 g of the expected compound, M.p.=286° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011154
Source datasetuspto-grants-2000_01
ORD IDord-35f61e6c851b4a0ea1452ff07497c43d
Source noteuspto-grants-2000_01