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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557033Generated: October 27, 2026

Methanol → 2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)-5-chlorobenzoic acid

https://huagongshe.com/reaction/557033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant4-(4-Chloro-2-cyano-phenyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 66757863—
Product2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)-5-chlorobenzoic acidHCID 66599565—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-(4-chloro-2-cyano-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (0.6 g, 1.86 mmol) in methanol (4.0 mL) was added 1.0 N NaOH (4.0 mL, 4.0 mmol) and the resulting mixture was heated to reflux at 80° C. for 36 h. Additional 1.0 N NaOH (2.0 ml, 2.0 mmol) was added to the reaction mixture and refluxed further for 18 hrs. The reaction mixture was concentrated and acidified to pH 4.0-5.0 using 1.0 N HCl and extracted with chloroform (5×). The combined organics were dried over sodium sulfate, concentrated and dried in vacuo overnight. The product contained approximately 20% amide and was separated after esterification in the next step. ESI-MS m/z: 341 (M+1), UV retention time: 2.33 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058287B2
Source datasetuspto-grants-2011_11
ORD IDord-5139c4d88e5646418d7bb05efe640707
Source noteuspto-grants-2011_11