HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 397371Erstellt: 23. Oktober 2026
Ethyl benzoate → 2-[2-(Methylsulfanyl)pyrimidin-4-yl]-1-phenylethan-1-one
https://huagongshe.com/de/reaction/397371
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl benzoate | HCID 7165 | — |
| Edukt | 4-Methyl-2-(methylsulfanyl)pyrimidine | HCID 821261 | — |
| Edukt | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-[2-(Methylsulfanyl)pyrimidin-4-yl]-1-phenylethan-1-one | HCID 12985829 | 99,5% |
Reaktionsschritte
86 ml (86 mmoles) of 1.0 M sodium bis(trimethylsilyl)amide in tetrahydrofuran was added drop-wise by addition funnel to a solution of 6.03 g (43 mmoles) 4-methyl-2-(methylthio)pyrimidine and 6.46 g (43 mmoles) ethyl benzoate in 86 ml tetrahydrofuran under a nitrogen atmosphere. After 2 hours the reaction was quenched with saturated ammonium chloride solution. Most of the tetrahydrofuran was removed in vacuo. The residue was diluted with 400 ml ethyl acetate and 200 ml water. The organic layer was separated and washed 2×100 ml saturated sodium chloride solution, separated, dried over Na2SO4, filtered, and concentrated in vacuo to give 10.45 g (42.77 mmoles) of 2-[2-(methyl thio)pyrimidin-4-yl]-1-phenyle thanone as a viscous red-brown oil that solidified upon standing. MH+=244.9.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06610697B1 |
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| Quelldatensatz | uspto-grants-2003_08 |
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| ORD ID | ord-6b5de7a632a44f69a9fe8f875b648dd4 |
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| Quellennotiz | uspto-grants-2003_08 |
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