Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26004Erstellt: 25. Oktober 2026

Phenol → Benzene, 1-(3-chloropropoxy)-4-(methylthio)-

https://huagongshe.com/reaction/26004

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
Edukt1-Bromo-3-chloropropaneHCID 8006—
Edukt4-(Methylthio)phenolHCID 14086—
EduktSodium hydrideHCID 24758—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktBenzene, 1-(3-chloropropoxy)-4-(methylthio)-HCID 1292862632%

Reaktionsschritte

A solution of 4-(methylthio)phenol (10.0 g, 0.071 mole) in 150 ml. of 1,2-dimethoxyethane is added to a slurry of a 57% dispersion of sodium hydride (3.0 g., 0.071 mole) in mineral oil (previously washed with hexane to remove the mineral oil) in 100 ml. of 1,2-dimethoxyethane. After the initial reaction is complete, 1-bromo-3-chloropropane (12.63 g., 0.08 mole) is added in one portion. The resulting mixture is stirred and refluxed for a period of 68 hrs., cooled and then concentrated under reduced pressure. Residual material (oil) is dissolved in ether and washed with water. The ether solution (after drying over magnesium sulfate) is concentrated under reduced pressure to provide 14.6 g. of an oil containing approximately 25% starting phenol according to NMR spectra. Distillation of the oil under reduced pressure affords, after a forerun of 4-(methylmercapto)phenol, 5.0 g. (32% yield) of 1-chloro-3-[4-(methylthio)phenoxy]propane, b.p. 150°-152° C. at 27 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04147805
Quelldatensatzuspto-grants-1979_04
ORD IDord-ef82afb4fb2e42d4ba1847aa4f491733
Quellennotizuspto-grants-1979_04