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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1106786Erstellt: 24. Oktober 2026

Sulfuric Acid → HCID 178520209, Verbindung

https://huagongshe.com/de/reaction/1106786

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
Eduktalpha-(1-Chlorocyclopropyl)-alpha-((2-chlorophenyl)methyl)-1H-1,2,4-triazole-1-ethanolHCID 119361—
EduktSulfurHCID 5362487—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktHCID 178520209HCID 17852020993%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

At -20° C., a mixture of 3.12 g (10 mmol) of 2-(1-chloro-cyclopropyl)-1-(2-chlorophenyl)-3-(1,2,4-triazol-1-yl)-propan-2-ol and 45 ml of absolute tetrahydrofuran is admixed with 8.4 ml (21 mmol) of n-butyllithium in hexane and stirred at 0° C. for 30 minutes. The reaction mixture is then cooled to -70° C., admixed with 0.32 g (10 mmol) of sulphur powder and stirred at -70° C. for 30 minutes. The mixture is warmed to -10° C., admixed with ice-water and adjusted to pH 5 by addition of dilute sulphuric acid. The mixture is extracted repeatedly with ethyl acetate and the combined organic phases are dried over sodium sulphate and concentrated under reduced pressure. In this manner, 3.2 g (93% of theory) of 2-(1-chloro-cyclopropyl)-1-(2-chlorophenyl)-3-(5-mercapto-1,2,4-triazol-1-yl)-propan-2-ol are obtained in the form of a solid substance which, after recrystallization, melts at 138-139° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06057353
Quelldatensatzuspto-grants-2000_05
ORD IDord-2caf5cbefd3844d9b722fa231dbb8fc8
Quellennotizuspto-grants-2000_05