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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869338Generated: October 31, 2026

HCID 68680161, compound → 4-Aminoindolin-2-one

https://huagongshe.com/reaction/1869338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68680161HCID 68680161—
CatalystIronHCID 23925—
SolventAcetic acid--water (1/1)HCID 21899381—
Product4-Aminoindolin-2-oneHCID 12237472—

Reaction Steps

4.43 g (18.45 mmol) of methyl-(2,6-dinitrophenyl)-acetate is added in 38.8 ml of glacial acetic acid and 11 ml of water and mixed with 3.75 g of iron powder and stirred for four more hours. In this case, heating to 40 to 60° C. takes place. The reaction mixture is added to ice water, mixed with ethyl acetate and vigorously stirred for ten minutes. The mixture is filtered through a glass-fiber filter, the organic phase is separated, and the aqueous phase is extracted twice more with ethyl acetate. The combined organic extracts are washed with brine, dried, and the solvent is spun off after the desiccant is filtered off. The residue is chromatographed on silica gel (mobile solvent methanol/dichloromethane). 2.38 g of 4-nitro-indol-2-one is isolated. The nitro compound is mixed again in glacial acetic acid/water with 2.7 g of iron powder, and the above-described cycle is passed through another time. 1.63 g of the desired amine is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638515B2
Source datasetuspto-grants-2009_12
ORD IDord-b14eddee36474d04923ffab6ddbd8b57
Source noteuspto-grants-2009_12