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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 255812Erstellt: 25. Oktober 2026

Formaldehyde → 1-(4-Chlorophenylthio)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-pentan-3-one

https://huagongshe.com/reaction/255812

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
Eduktp-ChlorothiophenolHCID 7815—
EduktPiperidineHCID 8082—
Edukt3,3-Dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanoneHCID 100877—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt1-(4-Chlorophenylthio)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-pentan-3-oneHCID 1319136528%

Reaktionsschritte

A mixture of 72.5 g (0.5 mol) of 4-chlorothiophenol, 100.2 g (0.6 mol) of 1,2,4-triazol-1-yl-pinacolin, 18 g (0.6 mol) of paraformaldehyde, 15 g of acetic acid and 5 ml of piperidine in 600 ml of toluene was heated under reflux in a water separator. After the water has been separated off, the reaction solution was washed with water, dried over sodium sulphate, filtered, and concentrated in vacuo. The oily residue was chromatographed over a silica gel column (mobile phase: chloroform). 45 g (28% of theory) of 1-(4-chlorophenylthio)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pentan -3-one of melting point 67° C. were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04699645
Quelldatensatzuspto-grants-1987_10
ORD IDord-928c673c32af4ee084ea5f08ee68500e
Quellennotizuspto-grants-1987_10