Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2051872Erstellt: 24. Oktober 2026

7-Benzoyl-3-methyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-one → 7-Benzoyl-3-methyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/de/reaction/2051872

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt7-Benzoyl-3-methyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-oneHCID 12909816—
KatalysatorHydroxy-nickelHCID 444642—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-Benzoyl-3-methyl-1,3-dihydro-2H-indol-2-oneHCID 1290124389%

Reaktionsschritte

A stirred solution of 8 g. (0.027 mole) of 7-benzoyl-3-methyl-3-methylthioindolin-2-one in 80 ml. of tetrahydrofuran was treated under N2 with 40 g. of a commercial Raney nickel-water mixture over a 2 hr. period. At the end of this period the mixture was filtered and the residue washed thoroughly with tetrahydrofuran. One drop of concentrated hydrochloric acid was added to the filtrate and the dark orange solution turned pale yellow. The solution was stripped under vacuum to a yellow oil which crystallized on seeding. The material was recrystallized from toluene petroleum ether to give a white crystalline material. The solid (6.0 g., 89% yield) melted at 125°-127° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04182774
Quelldatensatzuspto-grants-1980_01
ORD IDord-0a529a22acd64496b9c1dd17c77fac19
Quellennotizuspto-grants-1980_01