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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2318Erstellt: 24. Oktober 2026

Methane → 5-(4-Methylphenyl)-4,6-dichloro-2-(2-thienyl)pyrimidine

https://huagongshe.com/de/reaction/2318

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
Edukt2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
EduktThiopheneHCID 8030—
Edukt4,6-Dichloro-5-(4-methylphenyl)pyrimidineHCID 21979554—
EduktHCID 178418244HCID 178418244—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(4-Methylphenyl)-4,6-dichloro-2-(2-thienyl)pyrimidineHCID 1968950449,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of thiophene (1.69 g) in anhydrous tetrahydrofuran (20 ml) is added dropwise a 1.6M n-butyl lithium/n-hexane solution (11.4 ml) at 0° C. under argon atmosphere over a period of 30 minutes. To the mixture is added dropwise and gradually a solution of 5-(4-methylphenyl)-4,6-dichloropyrimidine (4.0 g) in anhydrous tetrahydrofuran (5 ml) at -60° C. The mixture is warmed to 0° C., and stirred for 1.5 hour. After the reaction is complete, to the mixture are added acetic acid (1.5 g) and water (0.25 g), and further added thereto a solution of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (5.70 g) in tetrahydrofuran (5 ml), and the mixture is stirred at 0° C. for one hour. The mixture is treated with an active charcoal, and extracted with a mixture of ethyl acetate and aqueous citric acid solution. The extract is washed, dried and evaporated to remove the solvent. The residue is purified by silica gel column chromatography (solvent; n-hexane/ethyl acetate=50:1) to give 5-(4-methylphenyl)-4,6-dichloro-2-(2-thienyl)pyrimidine (2.64 g) as powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728706
Quelldatensatzuspto-grants-1998_03
ORD IDord-1ce4869becc14147b48b50fb8a727e75
Quellennotizuspto-grants-1998_03