HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017613Generated: October 28, 2026
Acetic Acid → 4-(4-benzylpiperazin-1-yl)benzoic Acid
https://huagongshe.com/reaction/1017613
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-(4-Benzylpiperazin-1-yl)benzonitrile | HCID 8032691 | — |
| Product | 4-(4-benzylpiperazin-1-yl)benzoic Acid | HCID 4741724 | 38% |
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 wag 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, M30 ).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479497B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-6aba9a7af81841a78f1a82899e220eb0 |
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| Source note | uspto-grants-2002_11 |
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