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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416962Generated: October 31, 2026

Acetic Anhydride → 1-(2-Methyl-2,3-dihydroindol-1-yl)ethanone

https://huagongshe.com/reaction/2416962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-DimethylaminopyridineHCID 21885—
Reactant2-MethylindolineHCID 23305—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Product1-(2-Methyl-2,3-dihydroindol-1-yl)ethanoneHCID 4308221100%

Reaction Steps

To a mixture of 2-methylindoline (20.0 g, 0.15 mol) and dimethylaminopyridine (500 mg, 5 mmol) in pyridine (50 mL) at room temperature is added acetic anhydride (20 mL). The mixture is stirred at ambient temperature for 18 h, diluted with ethyl acetate, washed with 1 N aqueous hydrochloric acid, water and brine, then dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to give 26.3 g (100%) of the title compound as an amber oil. MS (ESI+) m/z 176.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825225B2
Source datasetuspto-grants-2004_11
ORD IDord-353f7cd7f2c3486f87111cc136a60ed1
Source noteuspto-grants-2004_11