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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645242Generated: November 1, 2026

Potassium Carbonate → N-benzyl-1-hydroxy-ethylamine

https://huagongshe.com/reaction/1645242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant4-(Piperidin-2-yl)butanoic acid--hydrogen chloride (1/1)HCID 12416327—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductN-benzyl-1-hydroxy-ethylamineHCID 18470673179.8%

Reaction Steps

4-Piperidin-2-ylbutanoic acid Hydrochloride (10.0 g, 48.3 mmol), and K2CO3 (26.6 g, 193.1 mmol) was dissolved in dest. water (70 ml) and Dioxane (124 ml). The reaction mixture was cooled to 0° C. and at this temperature Di-tert-butyldicarbonate (11.4 g, 53.1 mmol) was added slowly. The reaction mixture was stirred for 24 h at room temperature. After completion of the reaction water and Ethylacetate were added, the two phases were separated. The aqueous Phase was extracted once with Ethylacetate. Afterwards the aqueous Phase was triturated with 2 M HCL (aqueous) to reach pH=2. At this pH the aqueous phase was extracted 4× with Dichloromethane. The combined organic layers were dried over Magnesium sulfate, filtered out and evaporated to complete dryness to give (2) (13.13 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124624B2
Source datasetuspto-grants-2012_02
ORD IDord-ee14a51cc494414b9b203085a9257dd7
Source noteuspto-grants-2012_02