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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047367Generated: October 29, 2026

1-Boc-4-(3-(ethoxycarbonyl)phenyl)piperazine → 3-(4-(Tert-butoxycarbonyl)piperazin-1-yl)benzoic acid

https://huagongshe.com/reaction/2047367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(3-(ethoxycarbonyl)phenyl)piperazineHCID 16217941—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
Product3-(4-(Tert-butoxycarbonyl)piperazin-1-yl)benzoic acidHCID 4482872685.2%

Reaction Steps

A solution of 4-(3-ethoxycarbonyl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (5.00 g, 14.95 mmol) in EtOH (50 mL) and NaOH 10% (20 mL) was refluxed for 3 h, then the reaction mixture was cooled to room temperature and the organic solvent evaporated under reduced pressure. The resulting solution was neutralized by the dropwise addition of 1N HCl and the aqueous solution was extracted with EtOAc (3×50 mL) The combined organic layers were dried over Na2SO4, filtered, and concentrated under reduced pressure to obtain 3.90 g of the title compound (85%) without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592463B2
Source datasetuspto-grants-2013_11
ORD IDord-93898ce3a10a4e90865a4477ab808f3b
Source noteuspto-grants-2013_11