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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109622Generated: October 31, 2026

Sodium Acetate → 1-(3,3-Dimethyl-6-nitroindolin-1-yl)ethanone

https://huagongshe.com/reaction/2109622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantSodium FormateHCID 2723810—
ReactantN-(2-bromo-5-nitrophenyl)-N-(2-methylprop-2-en-1-yl)acetamideHCID 21959573—
CatalystTetraethylammonium ChlorideHCID 5946—
SolventDimethylformamideHCID 6228—
Product1-(3,3-Dimethyl-6-nitroindolin-1-yl)ethanoneHCID 16127418—

Reaction Conditions

Temperature80 °C

Reaction Steps

N-(2-Bromo-5-nitrophenyl)-N-(2-methylprop-2-enyl) acetamide (4.5 g, Step B) was dissolved in 50 mL anhydrous DMF, 2.5 g tetraethyl-ammonium chloride, 1.2 g sodium formate, 3 g sodium acetate were added, the resulting mixture was bubbled with nitrogen gas for 10 min. Pd(OAc)2 (350 mg) was added and the mixture was heated at 80° C. under N2 overnight. After the mixture was concentrated in vacuo, it was extracted between saturated NaHCO3 solution and EtOAc, the resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel with 2:1 Hexane:EtOAc to afford a yellow gum. MS: 235 (M+1). Calc'd. for C12H14N2O3−234.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514564B2
Source datasetuspto-grants-2009_04
ORD IDord-b05bc43d9d6b48f0b4e612e2cdb2135e
Source noteuspto-grants-2009_04