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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283625Generated: October 26, 2026

4-Benzoyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-one → 4-Benzoyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1283625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzoyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-oneHCID 12923552—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
Product4-Benzoyl-1,3-dihydro-2H-indol-2-oneHCID 12901246—

Reaction Steps

A stirred suspension of 7.0 g. (0.0248 mole) of 4-benzoyl-3-methylthioindolin-2-one in 400 ml. of tetrahydrofuran was treated portionwise under a nitrogen atmosphere with 35.0 g. of Raney nickel over a 2.5 hr. period. The reaction mixture was stirred for 1.5 hr. after addition was complete and the catalyst removed by filtration. The filter cake was washed well with tetrahydrofuran and methylene chloride and the filtrate evaporated under reduced pressure. The residue (5.6 g.) was recrystallized from methanol and gave 4.45 g. (76%) of product m.p. 210°-212°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975531
Source datasetuspto-grants-1976_08
ORD IDord-e38bbb3b10204703a8f0fa747b541232
Source noteuspto-grants-1976_08