HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1392589Erstellt: 25. Oktober 2026
Ethanolamine → 2-(benzyloxy)-N-(2-hydroxyethyl)benzamide
https://huagongshe.com/reaction/1392589
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanolamine | HCID 700 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 2-Benzyloxybenzoic acid | HCID 1810581 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(benzyloxy)-N-(2-hydroxyethyl)benzamide | HCID 56691307 | 101% |
Reaktionsschritte
1-(3-dimethylaminopropyl)3-ethylcarbodiimide hydrochloride (EDAC) (1.3 g, 6.57 mmol) was slowly added to a solution of 2-(phenylmethoxy)benzoic acid (1.5 g, 6.57 mmol), 1-hydroxybenzotriazole (HOBt) (0.89 g, 6.57 mmol), and ethanolamine (0.40 mL, 6.57 mmol) in 50 mL of anhydrous THF at 0° C. The suspension was stirred and warmed up slowly to room temperature over 24 hrs. The reaction mixture was concentrated to dryness under reduced pressure and the resulting residue was diluted with dichloromethane and washed with 0.5N HCl twice followed by the addition of a saturated NaHCO3 solution and brine. The organic layer was separated, dried through a MgSO4 pad and concentrated under reduced pressure to afford 1.8 g (100%) of N-(2-Hydroxyethyl)[2-(phenylmethoxy)phenyl]carboxamide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07342131B2 |
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| Quelldatensatz | uspto-grants-2008_03 |
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| ORD ID | ord-149f1bd19416463a83e36ade08e74e17 |
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| Quellennotiz | uspto-grants-2008_03 |
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