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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275007Generated: October 31, 2026

1-(6-Nitroindolin-1-yl)ethanone → 1-Acetyl-6-aminoindoline

https://huagongshe.com/reaction/1275007

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(6-Nitroindolin-1-yl)ethanoneHCID 258566—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product1-Acetyl-6-aminoindolineHCID 25856495%

Reaction Steps

A stirred suspension of 1-acetyl-2,3-dihydro-6-nitro-1H-indole (D9, 125 g, 0.61 mole) in THF (5500 ml) was hydrogenated over 10% Pd-C (20 g) at 50 psi for 20 h. The catalyst was removed by filtration through a plug of kieselguhr and the filtrate concentrated in vacuo to afford the title compound as a beige solid (102 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159979
Source datasetuspto-grants-2000_12
ORD IDord-cf38a93b1ec34dc4aa53d5c96bcf3c32
Source noteuspto-grants-2000_12