HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250240Generated: October 31, 2026
2-Nitrobenzaldehyde → 1-benzyl-N-[(2-nitrophenyl)methyl]piperidin-4-amine
https://huagongshe.com/reaction/2250240
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-benzyl-N-[(2-nitrophenyl)methyl]piperidin-4-amine | HCID 4848762 | 70% |
Reaction Steps
2-Nitrobenzaldehyde (1 g, 6.61 mmol) and 4-amino-1-benzylpiperidine (1.35 mL, 6.61 mmol) were combined in ethanol (20 mL). The resulting suspension was stirred at room temperature for 20 min before a solution of sodium borohydride (0.25 g, 6.61 mmol) in ethanol (5 mL) was added dropwise over 10 min. After the addition was complete, the reaction was stirred for 1 h, cooled to 0° C. and concentrated ammonium chloride was added to the reaction mixture until no bubbling was observed. The solvents were evaporated in vacuo and the resultant crude mixture was dissolved in water (10 mL) and methylene chloride (10 mL). The layers were separated and the organic layer washed with water (2×) and brine (2×), dried over sodium sulfate, filtered, and concentrated to afford 1.5 g (70%) of the desired product. LC/MS: tR=0.7 min, 326.18 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314883B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-0af7ccd993a54d5fb767546ec9e18ced |
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| Source note | uspto-grants-2008_01 |
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