Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086508Generated: October 26, 2026

N-Methyloxindole → 1,3-Dihydro-1-methyl-2H-indole-2-thione

https://huagongshe.com/reaction/1086508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethyloxindoleHCID 6096—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
Product1,3-Dihydro-1-methyl-2H-indole-2-thioneHCID 26156—

Reaction Steps

148 g (1.76 mol) of sodium bicarbonate are added in 20-gram portions with brisk stirring and at room temperature to a suspension of 130 g (0.8 mol) of 1-methyl-2-indolinone, prepared according to R. A. ABRAMOVITCH and D. H. HEY (J. Chem. Soc., 1954, 1699) and 133 g (0.3 mol) of phosphorus pentasulfide in 1.30 1 of anhydrous tetrahydrofuran. After 10 hours' stirring at room temperature, the mixture is filtered and the filtrate is concentrated on a water bath under vacuum. The residue is taken up with a water/ice mixture and the resulting mixture is extracted three times with chloroform. The organic phase is washed with water and then with saturated aqueous sodium chloride solution, dried and evaporated to dryness. The residue is recrystallized in methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05030646
Source datasetuspto-grants-1991_07
ORD IDord-b5fb62b22cfe47e3a699846361ca4946
Source noteuspto-grants-1991_07