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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637336Generated: November 1, 2026

Ethyl Acetate → 7-Acetyl-5-nitroindole

https://huagongshe.com/reaction/1637336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant7-Cyano-5-nitroindoleHCID 15453467—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product7-Acetyl-5-nitroindoleHCID 1554143426%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 7-cyano-5-nitroindole (0.7 g, 4.4 mmol) in 20 mL of THF was added 5.0 mL of MeMgBr (3.0 M) and the resulting reaction mixture was stirred for 12 h at 25° C. Reaction was quenched by adding 10 mL of 1.0 N aqueous HCl. Reaction mixture was basified with 3 N aqueous NaOH and aqueous solution was extracted with EtOAc several times. Organic extracts were dried over MgSO4 and concentrated in vacuo to provide oily residue which was subjected to column chromatography (50% EtOAc/Cy.hexane) to yield 0.20 g (1.2 mmol, 26%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040451
Source datasetuspto-grants-2000_03
ORD IDord-39345d7454704f4dae8c735ca49803a9
Source noteuspto-grants-2000_03