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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1704326Erstellt: 26. 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/reaction/1704326

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt7-Benzoyl-3-methyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-oneHCID 12909816—
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 nickelwater 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
PatentnummerUS04126635
Quelldatensatzuspto-grants-1978_11
ORD IDord-ecc835171d4e47e59a71ca986af1d4bc
Quellennotizuspto-grants-1978_11