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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907178Generated: October 25, 2026

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

https://huagongshe.com/reaction/907178

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) was suspended in EtOAc (200 mL). Pd/C (650 mg, 10%) was added, and the mixture was hydrogenated at 40-55 p.si.i. for 2 hours. The mixture was then filtered through celite. The filtrate was concentrated, and the residue was 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 numberUS08013006B2
Source datasetuspto-grants-2011_09
ORD IDord-211f6a2e7df249da86df1b907705f7e8
Source noteuspto-grants-2011_09