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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889994Generated: November 1, 2026

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

https://huagongshe.com/reaction/889994

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 anhydrous DMF (50 mL), tetraethyl-ammonium chloride (2.5 g), sodium formate (1.2 g), NaOAc (3 g) were added, and the resulting mixture was bubbled with N2 gas for 10 min. Pd(OAc)2 (350 mg) was added and the mixture was heated at 80° C. under N2 atmosphere overnight. After the mixture was concentrated in vacuo, it was partitioned 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 the title compound as a yellow gum. MS: 235 (M+1). Calc'd. for C12H14N2O3—234.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995162B2
Source datasetuspto-grants-2006_02
ORD IDord-bbe3179d1ddf467faab4ebdfffbaefa0
Source noteuspto-grants-2006_02