HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086392Generated: October 31, 2026
1-Phenylpiperazine → HCID 10293924, compound
https://huagongshe.com/reaction/2086392
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 22727321 | HCID 22727321 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10293924 | HCID 10293924 | 56.8% |
Reaction Steps
About 3 min after dissolving 3-[3-(3-nitrophenyl)isoxazol-5-yl]propanal (20 mg, 0.09 mmol) and 1-phenylpiperazine (13.4, 0.09 mmol) in 2 mL of dry methylene chloride, were added NaBH(OAc)3 (56 mg, 0.26 mmol) and molecular sieves (5 beads). After the reaction was carried out for about 22 hr, the reaction mixture was diluted with ethyl acetate and washed with saturated NaHCO3 solution saturated sodium chloride solution. After drying the organic layer over anhydrous MgSO4, the solvent was removed under reduced pressure. After dissolving the residue with 1 mL of diethyl ether, HCl ether solution was slowly dropped to precipitate a white hydrochloric acid salt which was collected by filtration or centrifugation, and it was washed several times with diethyl ether. After drying the same under reduced pressure, was obtained 18.1 mg (56.8%) of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06723724B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-4bb95affcf20468d9f7c9048ccd56342 |
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| Source note | uspto-grants-2004_04 |
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