HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024076Generated: October 29, 2026
1-(4-Nitrophenyl)piperazine → 1-(4-Nitrophenyl)-4-(oxetan-3-yl)piperazine
https://huagongshe.com/reaction/1024076
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(4-Nitrophenyl)piperazine | HCID 80447 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-Nitrophenyl)-4-(oxetan-3-yl)piperazine | HCID 86684152 | 76.1% |
Reaction Steps
To a mixture of 117c (2.0 g, 8.23 mmol), zinc chloride (2.2 g, 16.4 mmol), oxetan-3-one (1.18 g, 16.4 mmol) in methanol (80 mL) was added NaBH3CN (1.02 g, 16.4 mmol). The mixture was stirred at 50° C. for 5 hours. The mixture was then concentrated under reduced pressure and the residue was diluted with water (100 mL). It was extracted with dichloromethane (3×100 mL) and the combined organic layer was concentrated under reduced pressure. The residue was purified by silica-gel column chromatography eluting with 4:1 petroleum ether/ethyl acetate to afford 117d (1.65 g, 76%) as a yellow solid. MS: [M+H]+ 264.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722676B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-23338a47893f43129b7db68213723005 |
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| Source note | uspto-grants-2014_05 |
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