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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009608Generated: October 30, 2026

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

https://huagongshe.com/reaction/1009608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(6-Nitroindolin-1-yl)ethanoneHCID 258566—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product1-Acetyl-6-aminoindolineHCID 25856499%

Reaction Steps

1-Acetyl-6-nitroindoline (3.8 g, 18.3 mmol) is suspended in EtOAc (200 mL). Pd/C (650 mg, 10%) is added, and the mixture is hydrogenated at 40-55 p.si.i. for 2 hours. The mixture is then filtered through celite. The filtrate is concentrated, and the residue is triturated with ether to yield 1-acetyl-6-aminoindoline (3.18 g, 99%) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973069B2
Source datasetuspto-grants-2011_07
ORD IDord-b45a812ca19342b49f97767c9141a839
Source noteuspto-grants-2011_07