HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258821Generated: October 25, 2026
4-Nitrobenzyl chloride → 4-(Diphenylmethyl)-1-[(4-nitrophenyl)methyl]piperidine
https://huagongshe.com/reaction/258821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzyl chloride | HCID 7482 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Benzhydrylpiperidine | HCID 88278 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Diphenylmethyl)-1-[(4-nitrophenyl)methyl]piperidine | HCID 21424840 | — |
Reaction Steps
To a solution of 126 parts of 4-(diphenylmethyl)piperidine in 1200 parts of 95% ethanol is added a solution of 69 parts of sodium carbonate in 1500 parts of water. The resultant mixture is heated at the boiling point under reflux with vigorous stirring while a solution of 112 parts of 4-nitrobenzyl chloride in 800 parts of 95% ethanol is rapidly stirred in, and for 4 hours thereafter. Solvent is then removed by vacuum distillation, and the residue is partitioned between dichloromethane and water. The organic layer is separated, dried over anhydrous potassium carbonate, and stripped of solvent by vacuum distillation. The residue, recrystallized from anhydrous ethanol, affords 1-[(4-nitrophenyl)methyl]-4-(diphenylmethyl)piperidine melting at approximately 130°-131°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04035372 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-ebe4929252fc4946b215cba8f37f8399 |
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| Source note | uspto-grants-1977_07 |
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