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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244843Generated: October 31, 2026

Acetic Anhydride → 1-Acetyl-4-(acetyloxy)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1244843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 10465147HCID 10465147—
SolventTetrahydrofuranHCID 8028—
Product1-Acetyl-4-(acetyloxy)-1,3-dihydro-2H-indol-2-oneHCID 2022789027.4%

Reaction Steps

To a mixture of 4-(acetyloxy)-1,3-dihydro-2H-indol-2-one (J. Med. Chem., 38:2802–2808, 1995; 1.44 g, 7.5 mmol) and sodium carbonate (5.3 g, 50 mmol) in tetrahydrofuran (50 mL) is added acetic anhydride (4.3 mL, 45 mmol). The mixture is stirred at ambient temperature for 18 hours, and partitioned between ethyl acetate and water. After drying (magnesium sulfate), the solvent is removed in vacuo. The crude material is preadsorbed on silica gel (10 g), and purified by flash chromtography (90 g SiO2, 10% ethyl acetate:hexane to 70% ethyl acetate:hexane, linear gradient over 30 minutes) to provide 480 mg (27%) of acetic acid 1-acetyl-2-oxo-2,3-dihydro-1H-indol-4-yl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122680B2
Source datasetuspto-grants-2006_10
ORD IDord-1653a6ed7cd14d0a8cfd295030b3cc65
Source noteuspto-grants-2006_10