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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433911Generated: October 30, 2026

Acetic Acid → 4-(4-benzylpiperazin-1-yl)benzoic Acid

https://huagongshe.com/reaction/433911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
Reactant4-(4-Benzylpiperazin-1-yl)benzonitrileHCID 8032691—
Product4-(4-benzylpiperazin-1-yl)benzoic AcidHCID 474172438%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-(4-Benzylpiperazin-1-yl) benzonitrile (4.0 g, 15 mmol) was dissolved in glacial acetic acid (40 mL), 6 M hydrochloric acid (50 mL) was added and the reaction mixture was stirred at 100° C. for 17 h. The solvent was evaporated, the residue was suspended in water (10 mL) and the pH was adjusted to 3 by addition of 2 M sodium hydroxide (35 ml). The slurry was stirred at 50° C. for 2 h, cooled and the precipitate was filtered and dried in vacuo to give 4.1 g of a crude product. The solid was partitioned between methylene chloride (40 mL) and water (220 mL) with 2 M sodium hydroxide (8 mL). The aqueous phase was washed with methylene chloride (40 mL) and the pH was adjusted to 5 with 2 M hydrochloric acid. The aqueous phase was cooled, the precipitate was filtered and dried in vacuo to give 1.6 g (38% yield) of the title compound: mp 226° C. (dec); EIMS (70 eV) m/z (relative intensity) 296 (44, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670359B2
Source datasetuspto-grants-2003_12
ORD IDord-7df3b44caee94d2189561243862bc143
Source noteuspto-grants-2003_12