HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67063Generated: October 29, 2026
Salicylaldehyde → 2-(((1-Benzylpiperidin-4-yl)amino)methyl)phenol
https://huagongshe.com/reaction/67063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(((1-Benzylpiperidin-4-yl)amino)methyl)phenol | HCID 4792504 | 80.7% |
Reaction Steps
In this reference example, 9.76 g of salicylaldehyde, 15.12 g of 1-benzyl-4-amino-piperidine and 100 ml of methanol are mixed and stirred at room temperature for one hour. While the resultant mixture is cooled with ice, 3.2 g of sodium borohydride is added thereto over a period of one hour and 30 minutes. Then, the mixture is stirred at room temperature for 2 hours. The resultant reaction mixture is poured into 1 l of ice water. The light yellow crystals deposited are separated by filtration and then dissolved in 200 ml of ethyl acetate. The ethyl acetate solution is washed with a saturated aqueous sodium chloride, dried and subsequently concentrated under reduced pressure to obtain 19.0 g of light yellow crystals. The crystals are recrystallized from ethanol to obtain 12.0 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04344945 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-ea407051a732415e85d81bf46a8b64a6 |
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| Source note | uspto-grants-1982_08 |
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