HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017685Generated: October 31, 2026
1-(4-Nitrophenyl)piperazine → HCID 18403833, compound
https://huagongshe.com/reaction/1017685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(4-Nitrophenyl)piperazine | HCID 80447 | — |
| Reactant | HCID 4064704 | HCID 4064704 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 18403833 | HCID 18403833 | 86% |
Reaction Steps
To a solution of 3-methoxy-4-(methylaminocarbonyloxy)benzaldehyde (1.01 g) in 1,2-dichloroethane (19.0 ml) was added 1-(4-nitrophenyl)piperazine (1.0 g), and sodium triacetoxyborohydride (1.54 g), with stirring. The reaction mixture was stirred for 3 hrs at ambient temperature, poured into ice/saturated sodium carbonate solution (100 ml) and extracted with dichloromethane. The combined organic extracts were washed with water and brine, dried over sodium sulfate, filtered, and the filtrate was concentrated. The residue was flash chromatographed (silica gel), eluting with dichloromethane, followed by 1% methanol:dichloromethane. The appropriate fractions were collected and concentrated to give 1.66 g (86%) of product. Recrystallization from ethyl acetate gave the analytical sample, mp 155-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479495B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-426a0a58db0645b7aeb460946f838425 |
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| Source note | uspto-grants-2002_11 |
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