HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44166Erstellt: 24. Oktober 2026
Dicyclohexylcarbodiimide → 4-Carbamoylphenyl 2-(2-methoxynaphthalen-6-yl)propanoate
https://huagongshe.com/de/reaction/44166
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | 4-Hydroxybenzamide | HCID 65052 | — |
| Edukt | Naproxen | HCID 156391 | — |
| Edukt | HCID 178418300 | HCID 178418300 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-Carbamoylphenyl 2-(2-methoxynaphthalen-6-yl)propanoate | HCID 59345593 | 32% |
Reaktionsschritte
To the solution of 1 (naproxen, 4 g, 17.4 mmol) in 80 mL of dimethylformamide, hydroxybenzotriazole (2.59 g, 19.14 mmol) and DCC (2.59 g, 19.14 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxybenzamide (4, 3.58 g, 26.1 mmol) was added and stirred for 1 h at 0° C. and 2 h at room temperature. After filtration, the filtrate was evaporated under reduced pressure to remove the solvent. The oily residue thus obtained was dissolved in ethyl acetate; the organic layer was washed with brine, with NaHCO3 5%, with citric acid 10% and than dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product 5 was loaded on a silica gel open column and eluted with CH2Cl2/MeOH (9.5/0.5), from which 4-carbamoylphenyl 2-(2-methoxynaphthalen-6-yl)-propanoate (5) was obtained (1.91 g, 32% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541398B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-bf5b7215cf1a4ccc83d7a4850936d780 |
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| Quellennotiz | uspto-grants-2013_09 |
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