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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38485Generated: October 25, 2026

Acetic Anhydride → 1-(5-Bromo-3-methyl-1H-indazol-1-yl)ethan-1-one

https://huagongshe.com/reaction/38485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantIsoamyl NitriteHCID 8053—
Reactant18-Crown-6HCID 28557—
ReactantPotassium AcetateHCID 517044—
Reactant4-Bromo-2-ethylanilineHCID 2801283—
SolventChloroformHCID 6212—
Product1-(5-Bromo-3-methyl-1H-indazol-1-yl)ethan-1-oneHCID 59127382—

Reaction Steps

Acetic anhydride (4.73 ml) was added to the mixture of 4-bromo-2-ethylaniline (5.0 g) and KOAc (2.94 g) in CHCl3 (70 ml) and stirred for 30 minutes at reflux. Then isoamyl nitrite (6.65 ml) and 18-crown-6-ether (660 mg) was added to the reaction mixture and stirred for 12 h. under reflux. The reaction mixture was diluted with CHCl3, washed with water, and dried over sodium sulfate. After filtration and concentration, the residue was purified by silica gel chromatography (hexane/EtOAc), and crystallized from mixed solvent of hexane and CHCl3 to give intended compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524730B2
Source datasetuspto-grants-2013_09
ORD IDord-7b5dffd064424629bd0d34f8d159136b
Source noteuspto-grants-2013_09