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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862190Generated: October 29, 2026

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

https://huagongshe.com/reaction/862190

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 8 h. 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 6.7 g of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05717100
Source datasetuspto-grants-1998_02
ORD IDord-2021657eb85f450a97a793f837ae6338
Source noteuspto-grants-1998_02