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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991499Generated: November 1, 2026

Hydrochloric Acid → 1-((Tert-butoxy)carbonyl)-4-phenylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/991499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Phenylpiperidine-4-carboxylic acid, compound with toluene-p-sulphonic acidHCID 19259—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product1-((Tert-butoxy)carbonyl)-4-phenylpiperidine-4-carboxylic acidHCID 736917—

Reaction Conditions

Temperature60 °C

Reaction Steps

Place 100 g of 4-phenylpiperidine-4-carboxylic acid and p-toluenesulphonic acid in 800 ml of dioxane, add 150 ml of water and 109.7 g of K2CO3. Heat to 60° C. then add, drop by drop, 60.7 g of (Boc)20 in 100 ml of dioxane. Leave for 4 hours with stirring at 60° C. then heat under reflux for 1 hour. Evaporate to dryness, take up the solid formed in water, acidify to a pH of 3 by the addition of 2 N HCl, then add ether. Filter the crystals formed, wash them in water then in ether. Evaporate the etherified filtrate to dryness, take up the residue in ether and filter the crystals formed and add to those already obtained in order to dry them. 71 g of the desired compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465489B1
Source datasetuspto-grants-2002_10
ORD IDord-3799ff22e5c5452aab8dc03b0a5fe9b3
Source noteuspto-grants-2002_10