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

HRID 262289

Reaktionsgleichung

Reaktionsgleichung von HRID 262289
[C:1]1([C:7]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[NH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>Cl.[Zn]>[C:1]1([CH:7]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[NH:9][CH2:8]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Komponenten

4

Edukt 1

HCID 965023-Phenylindole

Produkt 1

HCID 109323533-phenyl-2,3-dihydro-1H-indole

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23994ZincKatalysator2×HCID 313Hydrochloric AcidLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

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.

Aufarbeitung

  1. temperaturethe reaction mixture was heated to 100° C.
  2. temperaturemaintained at this temperature for one hour
  3. filtrationfiltered hot
  4. temperaturethe filtrate cooled to room temperature
  5. washwashed with ether
  6. extractionthe desired product was extracted with ether
  7. custompurified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-408e9a76d31647578c20129546c09678
Quelldatensatz
uspto-grants-1979_05
Patentnummer
US04153789

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