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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4476Erstellt: 23. Oktober 2026

1-(2,3-Dihydro-1H-indol-7-yl)ethan-1-one → 1-(1H-indol-7-yl)ethanone

https://huagongshe.com/de/reaction/4476

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(2,3-Dihydro-1H-indol-7-yl)ethan-1-oneHCID 13699421—
KatalysatorHCID 178418406HCID 178418406—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(1H-indol-7-yl)ethanoneHCID 1377053476%

Reaktionsschritte

To 30 g. (0.186 mole) of 7-acetylindoline in 415 ml. of methylene chloride was added 48.5 g (0.56 mole) of manganese dioxide and the mixture refluxed through a soxhlet filled with 4A molecular sieves for 22 hours. The mixture was cooled and an additional 48.5 g. of manganese dioxide was added. Fresh molecular sieves were added and the refluxing continued for 5 hours. The same amount of manganese dioxide and molecular sieves were added again and the refluxing was continued for one hour. The mixture was filtered and the filtrate concentrated to dryness. The residue was triturated with hexane and filtered, 22.57 g. (76% yield), m.p. 65°-66° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04725616
Quelldatensatzuspto-grants-1988_02
ORD IDord-72e6c5070b794368854183d6caa959fa
Quellennotizuspto-grants-1988_02