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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | 4-(Piperidin-2-yl)butanoic acid--hydrogen chloride (1/1) | HCID 12416327 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-benzyl-1-hydroxy-ethylamine | HCID 18470673 | 179.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124624B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-ee14a51cc494414b9b203085a9257dd7 |
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| Source note | uspto-grants-2012_02 |
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