Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | 1,4-Bis(3-aminopropyl)piperazine | HCID 81629 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11711391 | HCID 11711391 | — |
Reaction Steps
To a solution of 1,4-bis(3-aminopropyl)piperazine (0.51 mL, 2.5 mmol) and 4-fluorobenzaldehyde (0.59 mL, 5.5 mmol) in absolute ethanol (20 mL), 3 Å molecular sieves are added. After stirring the mixture at room temperature for 5 h, NaBH (0.47 g, 12.5 mmol) was added portionwise and the mixture was stirred for 12 h at room temperature. The reaction 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). Combined organic layers were extracted with HCl 1M. The combined aqueous layers were neutralized with NaOH 1M and extracted with CH2Cl2. Combined organic layers were dried over MgSO4. Crude compound is purified thick-layer chromatography (acetone/NH4OH: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-25b8026614bb4f15a6f333d3d05f4ce8 |
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| Source note | uspto-grants-2015_06 |
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