HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18635Erstellt: 24. Oktober 2026
Dicyclohexylcarbodiimide → 4-(Isothiocyano)-phenyl 2-(2-methoxynaphthalen-6-yl)propanoate
https://huagongshe.com/de/reaction/18635
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | Naproxen | HCID 156391 | — |
| Edukt | Desmethylanethol trithione | HCID 3082127 | — |
| Edukt | HCID 178418300 | HCID 178418300 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-(Isothiocyano)-phenyl 2-(2-methoxynaphthalen-6-yl)propanoate | HCID 25065769 | 21% |
Reaktionsschritte
To the solution of 1 (naproxene, 691 mg, 3 mmol) in 20 mL of dimethylformamide, hydroxybenzotriazole (446 mg, 3.3 mmol) and DCC (619 mg, 3.3 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxyphenylisothiocyanate (2; 500 mg, 3.3 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 and the precipitate was removed. The solvent was evaporated and the crude product was loaded on a silica gel open column and eluted with dichloromethane, from which 4-(isothiocyano)-phenyl 2-(2-methoxynaphthalen-6-yl)propanoate (3) was obtained (230 mg, 21% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741359B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-ff81df212f994bafbf6c7bfe90e1cc54 |
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| Quellennotiz | uspto-grants-2010_06 |
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