HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563145Generated: October 29, 2026
4-Butoxybenzaldehyde → HCID 59808329, compound
https://huagongshe.com/reaction/563145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Butoxybenzaldehyde | HCID 79813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67005485 | HCID 67005485 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59808329 | HCID 59808329 | 67.2% |
Reaction Steps
2-Amino-1-(4-benzyl-piperazin-1-yl)-(S)-3-phenyl-propan-1-one hydrochloride (500 mg, 1.26 mmol) were dissolved in MeOH (5 mL), DIPEA (359 mg, 2.77 mmol) and 4-n-butoxybenzaldehyde (226 mg, 1.26 mmol) was added and the mixture was heated to reflux for 2 h, cooled again to rt followed by slow addition of sodium borohydride (48 mg, 1.26 mmol) in portions. Stirring was continued for 15 min. Water (1 mL) was added and the solvents were removed under reduced pressure. The residue was taken up in diethylether (5 mL), washed with 10% aq. citric acid (5 mL) and water (5 mL), dried over magnesium sulfate, filtered and concentrated in vacuo to give 411 mg (67%) of 1-(4-benzyl-piperazin-1-yl)-2-(4-butoxy-benzylamino)-(S)-3-phenyl-propan-1-one. LC-MS: tR=0.74 min; [M+H]+=486.43.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067419B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-edc50b27b88c4e86aea8c5d833b9b7b9 |
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| Source note | uspto-grants-2011_11 |
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