HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1164985Erstellt: 25. Oktober 2026
Triethylamine → Methyl 2-[2-Hydroxy-3-[N-[2-[N-(phenylaminocarbonyl)amino]ethyl]amino]propoxy]benzoate
https://huagongshe.com/reaction/1164985
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methyl 2-(oxiran-2-ylmethoxy)benzoate | HCID 279510 | — |
| Edukt | 3-(2-Aminoethyl)-1-phenylurea hydrochloride | HCID 19863750 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Methyl 2-[2-Hydroxy-3-[N-[2-[N-(phenylaminocarbonyl)amino]ethyl]amino]propoxy]benzoate | HCID 13030944 | 7,5% |
Reaktionsschritte
4.8 g of N-phenyl-N'-(2-aminoethyl)urea HCl salt (0.024 mole) was placed in 100 ml of methanol, and 2.5 g of triethylamine (0.024 mole) was added. While this reaction mixture was being stirred, a solution of 5 g of methyl 2-(2,3-epoxypropoxy)benzoate (0.024 mole) in 25 ml methanol was added slowly. The solution was then heated to reflux for 4 hours. The methanol was removed under reduced pressure and the resulting gel-like solid was dissolved in 100 ml of methylene chloride. The organic layer was washed twice with 100 ml of water and dried over anhydrous magnesium sulfate. Removal of the methylene chloride left an oil which was dissolved in 50 ml of methanol/ethyl ether (1:1) from which the product crystallized slowly upon refrigeration to afford 0.7 g (7.5%) of product having a melting point of 133°-134° C. The compound was identified by its NMR spectrum and elemental analysis.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04906661 |
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| Quelldatensatz | uspto-grants-1990_03 |
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| ORD ID | ord-c10f3505907744b89d2b71a5cc55d86d |
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| Quellennotiz | uspto-grants-1990_03 |
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