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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2233747Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3-(4-chlorophenoxy)-2-methyl-5-(methylthio)-1H-indole

https://huagongshe.com/de/reaction/2233747

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt1-(4-Chlorophenoxy)acetoneHCID 239874—
Edukt(4-(Methylsulfanyl)phenyl)hydrazine hydrochlorideHCID 2760977—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-(4-chlorophenoxy)-2-methyl-5-(methylthio)-1H-indoleHCID 68617147—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

1-(4-Chloro-phenoxy)-propan-2-one (2.66 g) was added to a stirred solution of [4-(methylthio)phenyl]-hydrazine hydrochloride (2.5 g) in MeCN (15 ml)/HCl (0.5M, 15 ml) at RT. The reaction was stirred at 50° C. for 1 h. After cooling to room temperature, the reaction was partitioned between ethylacetate/water, the organics were separated, washed with aq sodium hydroxide (1 M), dried and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 5-20% ethylacetate/iso-hexane. The resulting hydrazone was dissolved in THF (80 ml). Sodium bicarbionate solid (1.04 g) was added followed by phosphorus trichloride (0.41 ml) dropwise, and the reaction stirred at RT for 2 h. Further phosphorus trichloride (1.20 ml) was added dropwise, and the reaction stirred at RT for 16 h. The reaction was quenched with water. The mixture was extracted with ethylacetate, the organics washed with aq. sodium hydrogencarbonate, brine, dried and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 5-10% ethylacetate/iso-hexane. Yield 0.45 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07709521B2
Quelldatensatzuspto-grants-2010_05
ORD IDord-b92b96d35dcd4878af312445a5f834de
Quellennotizuspto-grants-2010_05