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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product2-(((1-Benzylpiperidin-4-yl)amino)methyl)phenolHCID 479250480.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04344945
Source datasetuspto-grants-1982_08
ORD IDord-ea407051a732415e85d81bf46a8b64a6
Source noteuspto-grants-1982_08