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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 262289Erstellt: 25. Oktober 2026

3-Phenylindole → 3-phenyl-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/262289

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-PhenylindoleHCID 96502—
KatalysatorZincHCID 23994—
LösungsmittelHydrochloric AcidHCID 313—
Produkt3-phenyl-2,3-dihydro-1H-indoleHCID 10932353—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

1.3 G of 3-phenylindole was suspended in 100 ml of 20% aqueous hydrochloric acid. The mixture was heated to 60° C. while stirring vigorously and 20 g of zinc dust was added thereto in small portions over a period of 45 minutes. On completing the addition of zinc dust, the reaction mixture was heated to 100° C. and maintained at this temperature for one hour, filtered hot, and the filtrate cooled to room temperature and washed with ether. The aqueous layer was basified with 50% aqueous sodium hydroxide and the desired product was extracted with ether and then purified by column chromatography using silica gel. The 3-phenylindoline was obtained in a yield of 0.8 g as a yellow viscous oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04153789
Quelldatensatzuspto-grants-1979_05
ORD IDord-408e9a76d31647578c20129546c09678
Quellennotizuspto-grants-1979_05