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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 81701Erstellt: 25. Oktober 2026

Sodium Hydroxide → 3-Chloro-4-[(2-chloropyrimidin-4-yl)thio]-2-methylaniline

https://huagongshe.com/reaction/81701

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt2,4-DichloropyrimidineHCID 77531—
EduktSodium borohydrideHCID 4311764—
EduktSodium hydrosulfide hydrateHCID 16211346—
Edukt3-Chloro-2-methyl-4-thiocyanatoanilineHCID 37859309—
LösungsmittelMethanol--water (1/1)HCID 22242641—
Produkt3-Chloro-4-[(2-chloropyrimidin-4-yl)thio]-2-methylanilineHCID 5949167451,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Crude 4-amino-2-chloro-3-methylphenyl thiocyanate (600 mg, 3.0 mmol) was dissolved in a mixture of methanol:water (2:1, 22 mL) and cooled to 0° C. Sodium hydrosulfide monohydrate (338 mg, 4.6 mmol) and sodium borohydride (447 mg, 11.8 mmol) were added then the mixture was allowed to warm to room temperature and stir overnight. After this time sodium hydroxide (96 mg, 2.4 mmol) was added followed by 2,4-dichloropyrimidine (360 mg, 2.4 mmol) and the mixture allowed to stir for a further 24 h. The methanol was removed in vacuo and then the mixture was extracted with ethyl acetate. The extracts were dried (Na2SO4) and evaporated then the residue was purified by flash chromatography to afford 3-chloro-4-[(2-chloropyrimidin-4-yl)thio]-2-methylaniline (353 mg, 41%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846704B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-4ade47deac6c4594a6d8c90bd28d38c0
Quellennotizuspto-grants-2014_09