HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907577Generated: October 29, 2026
Water → 2-Piperazin-1-yl-benzoic acid sulfuric acid salt
https://huagongshe.com/reaction/907577
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | N-(2-Cyanophenyl)piperazine | HCID 2735875 | — |
| Product | 2-Piperazin-1-yl-benzoic acid sulfuric acid salt | HCID 67388050 | — |
Reaction Steps
1-(2-Cyanophenyl)piperazine (2.00 g, 10.68 mmol) was suspended in 10 mL of concentrated sulfuric acid. The piperazine slowly dissolved as the reaction mixture was heated to 100° C. After heating the reaction for 2 hr, the reaction was cooled to room temperature. 10 mL of water was added and the reaction was heated to 100° C. for another 4 hr. After cooling to room temperature, the reaction mixture was poured into 200 mL of ice water. The aqueous mixture was neutralized with ammonium hydroxide and the mixture was concentrated under vacuum. The product was extracted from the inorganic salts by washing with 25% methanol in tetrahydrofuran. The crude material was used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08013156B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-a0c7bb0dc7814a95ab0140e37799f5cd |
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| Source note | uspto-grants-2011_09 |
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