HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 237123Erstellt: 25. Oktober 2026
Trifluoroacetic acid → Ethyl 6-ethyl-3,4-dihydro-5-hydroxy-4-oxothieno[2,3-d]PYRIMIDINE-2-CARBOXYLATE
https://huagongshe.com/reaction/237123
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | Ethyl 5-amino-6-ethyl-3,4-dihydro-4-oxothieno[2,3-d]PYRIMIDINE-2-CARBOXYLATE | HCID 12516925 | — |
| Edukt | Potassium trifluoroacetate | HCID 23662811 | — |
| Produkt | Ethyl 6-ethyl-3,4-dihydro-5-hydroxy-4-oxothieno[2,3-d]PYRIMIDINE-2-CARBOXYLATE | HCID 23330393 | — |
Reaktionsschritte
The diazonium fluoborate salt is prepared as in Procedure 63 from the amino compound produced in Procedure 51 yielding 0.03 mole of the required diazonium fluoborate. The latter is added in one portion to a solution of 0.03 mole of potassium trifluoroacetate in 13 ml. of trifluoroacetic acid at 0° C. The mixture is stirred at 25° C. for one hour and then refluxed overnight. The trifluoroacetic acid is evaporated in vacuo to give a residue which is triturated with water and filtered to give the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04159377 |
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| Quelldatensatz | uspto-grants-1979_06 |
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| ORD ID | ord-b5eceba6e9d445f4bc3d61216a917bed |
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| Quellennotiz | uspto-grants-1979_06 |
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