HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486751Generated: October 28, 2026
Hydrochloric Acid → (+/-)-1,4-Bis(diphenylcarbamoyl)piperazine2-carboxylic acid
https://huagongshe.com/reaction/486751
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N,N-Diphenylcarbamic chloride | HCID 65741 | — |
| Reactant | Piperazine-2-carboxylic acid dihydrochloride | HCID 2723757 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (+/-)-1,4-Bis(diphenylcarbamoyl)piperazine2-carboxylic acid | HCID 22004705 | 26% |
Reaction Steps
A solution of 946 mg (4 mmole) of 98% diphenylcarbamoyl chloride in 4 ml of acetonitrile was added dropwise to a stirring solution of 406.2 mg (2 mmole) of piperazine-2-carboxylic acid dihydrochloride [E. Felder, S. Maffei, S. Pietra and D. Pitre, Helv. Chim., Acta. 43, 888 (1960)] in 4 ml of 2.5N-sodium hydroxide at a temperature between 0° and 5° C. After the addition was completed, the stirring was continued for 4 hours and the solution was acidified with 2N-hydrochloric acid while cooling in an ice bath. The reaction mixture was concentrated under reduced pressure and the residue was extracted with chloroform. After washing with water, the chloroform solution was dried over MgSO4 and concentrated in vacuo. The only product which solidified on cooling was triturated with isopropyl ether to give 270 mg (26%) of (±)-1,4-bis(diphenylcarbamoyl)piperazine2-carboxylic acid, m.p. 244°-246° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292726 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-e4ed22f95ff544038c73676c772e5fa1 |
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| Source note | uspto-grants-1994_03 |
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