HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883571Generated: October 30, 2026
Acetic Acid → 1-(3-Chloro-4-nitrobenzyl)-4-methylpiperazine
https://huagongshe.com/reaction/883571
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 3-Chloro-4-nitrobenzaldehyde | HCID 3769779 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(3-Chloro-4-nitrobenzyl)-4-methylpiperazine | HCID 57538944 | 71.2% |
Reaction Steps
N-methyl piperazine (2.50 mL, 22.5 mmol) was added dropwise to a solution of 3-chloro-4-nitrobenzaldehyde (2.09 g, 11.3 mmol) and acetic acid (0.29 mL, 5.14 mmol) in toluene (11.7 mL) at room temperature. The reaction mixture was stirred for 1.5 h at room temperature before the addition of further toluene (4.4 mL) and sodium triacetoxyborohydride (3.58 g, 16.9 mmol). The reaction mixture was stirred at room temperature overnight and then quenched by the addition of MeOH (3 mL) and saturated aqueous NaHCO3 (23 mL). The reaction mixture was stirred for 30 min. The phases were separated and the aqueous layer was extracted with toluene (2×30 mL). The combined organic extracts were concentrated under reduced pressure and purified by flash column chromatography (EtOAc:MeOH:NEt3 9:1:0.1) to give the title compound (2.17 g, 71%) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236954B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-fa22004cb70549f4aaf780cadbcd0b24 |
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| Source note | uspto-grants-2012_08 |
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