HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112738Generated: November 4, 2026
1-Phenylpiperazine → HCID 22762587, compound
https://huagongshe.com/reaction/1112738
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 22762545 | HCID 22762545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22762587 | HCID 22762587 | — |
Reaction Steps
A solution of N-phenacyl-3-bromopropanamide (10.2 g; 0.038 mole) and N-phenylpiperazine (12.0 g; 0.074 mole) in dry DMF (100 ml) was stirred with anhydrous, finely-powdered sodium carbonate (15.0 g) for 18 hours at room temperature. The temperature was then increased to 80° C. and held for 12 hours to complete the reaction. The DMF was evaporated off under vacuum and the residue diluted with water (100 ml). The mixture was extracted with chloroform (3 × 100 ml). The extracts were shaken with 2 × 100 ml 2N HCl and the organic layer discarded. The aqueous layer was basified with NaOH solution to pH 9 and extracted with 3 × 75 ml CHCl3. The extracts were washed with water and dried. After removal of the solvent the remaining viscous gum triturated with ether to give a buff-coloured solid. After recrystallisation from isopropanol the product weighed 6.0 g and melted at 126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04123529 |
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| Source dataset | uspto-grants-1978_10 |
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| ORD ID | ord-ab5c6fe7e50e4cf4bedafb686dac64ff |
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| Source note | uspto-grants-1978_10 |
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