HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 453105Erstellt: 27. Oktober 2026
Ethyl cyanoformate → 3-(4-Benzyloxyphenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester
https://huagongshe.com/reaction/453105
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl cyanoformate | HCID 69336 | — |
| Edukt | 5-(4-Benzyloxyphenyl)-[1,3,4]oxathiazol-2-one | HCID 59549525 | — |
| Lösungsmittel | 1,2-Dichlorobenzene | HCID 7239 | — |
| Produkt | 3-(4-Benzyloxyphenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester | HCID 59549532 | 68% |
Reaktionsschritte
To a solution of 5-(4-benzyloxyphenyl)-[1,3,4]oxathiazol-2-one (0.31 g, 1.08 mmol) in 1,2-dichlorobenzene (2 ml) was added ethyl cyanoformate (0.43 ml, 4.35 mmol). The resulting reaction mixture was refluxed overnight at 150° C. After the completion of the reaction (TLC monitoring), added ice-cold water and extracted with ethyl acetate (3×50 ml). The combined organic layer was dried over Na2SO4, filtered and concentrated under vacuum, to get the product (0.250 g, 65%). MS ES+ (341.12).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08492414B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-d8a75c907c1b4e628f176109b22bb1bc |
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| Quellennotiz | uspto-grants-2013_07 |
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