HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167075Generated: October 31, 2026
4-Nitrobenzaldehyde → HCID 11705489, compound
https://huagongshe.com/reaction/2167075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Bis(3-aminopropyl)piperazine | HCID 81629 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11705489 | HCID 11705489 | — |
Reaction Steps
To a solution of 1,4-bis(3-aminopropyl)piperazine (0.513 mL, 2.49 mmol) and 4-nitrobenzaldehyde (792 mg, 5.24 mmol) in absolute ethanol (20 mL) was added 3 Å molecular sieves (5 g). After stirring the mixture for 12 h at room temperature, sodium borohydride (1.9 g, 49.9 mmol) was added and the mixture was stirred for 12 h under reflux. Then the reaction mixture was quentched by dropwise addition of water (20 mL) and ethanol was removed under reduced pressure. The aqueous residue was extracted with CH2Cl2 (3×30 mL) and the combined organic layers were extracted with HCl 1N (2×50 mL). The combined aqueous layers were neutralized with NaOH 1N (50 mL) and extracted with CH2Cl2 (3×30 mL). The combined organic layers were dried over MgSO4, evaporated to dryness and the oily residue purified by flash chromatography (neutral aluminium oxide, CH2Cl2/MeOH: 90/10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09044478B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-c4bec7fbe02f4283bf5f0d772885545f |
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| Source note | uspto-grants-2015_06 |
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