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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl benzoateHCID 7165—
Edukt4-Methyl-2-(methylsulfanyl)pyrimidineHCID 821261—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-[2-(Methylsulfanyl)pyrimidin-4-yl]-1-phenylethan-1-oneHCID 1298582999,5%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06610697B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-6b5de7a632a44f69a9fe8f875b648dd4
Quellennotizuspto-grants-2003_08