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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287420Generated: October 31, 2026

Acetic Acid → 4-Benzyl-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/2287420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
Reactant1-tert-Butyl 4-ethyl 4-benzylpiperidine-1,4-dicarboxylateHCID 16218271—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyl-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acidHCID 1215102066.4%

Reaction Steps

To a stirring solution of 4-benzylpiperidine-1,4-dicarboxylic acid tert-butyl ester ethyl ester (31.6 mmol, 11.01 g) in isopropyl alcohol (50 mL) and THF (50 mL) was added 3N NaOH (63.4 mmol, 21.1 mL) and the biphasic solution was heated to reflux. The reaction was heated for 8h. and then left stirring at room temperature overnight. The reaction was then diluted with water (200 mL) and acidified to pH=4 with glacial acetic acid. The aqueous mixture was then extracted with ethyl acetate (2×500 mL). The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, and evaporated under reduced pressure. The resulting solid was triturated with diethyl ether to give 6.7g of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083949
Source datasetuspto-grants-2000_07
ORD IDord-67bce80067e049fca4dcee52af935610
Source noteuspto-grants-2000_07