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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34127Generated: October 26, 2026

Acetic Anhydride → 1-(5-bromo-6-fluoro-1H-indazol-1-yl)ethanone

https://huagongshe.com/reaction/34127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantIsoamyl NitriteHCID 8053—
ReactantPotassium AcetateHCID 517044—
ReactantN-(4-Bromo-5-fluoro-2-methylphenyl)acetamideHCID 23070217—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product1-(5-bromo-6-fluoro-1H-indazol-1-yl)ethanoneHCID 59694475—

Reaction Steps

To a solution of 77.0 g of N-(4-bromo-5-fluoro-2-methylphenyl)acetamide in 930 mL of toluene were added 93.0 mL of acetic anhydride and 37.0 g of potassium acetate at room temperature, and the resultant solution was heated at 90° C., slowly added dropwise with 67.0 mL of isoamyl nitrite, and stirred at this temperature for 3 hours. After diluting with ethyl acetate, washing successively with water and saturated brine, and drying over anhydrous magnesium sulfate, the solvent was evaporated. The precipitated crystals were washed with diethyl ether:n-hexane=1:10, the filtrate concentrated and purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=0:100-1:5) and finally combined with the previous crystals, to afford 22.5 g of the title compound as pale brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429609B2
Source datasetuspto-grants-2008_09
ORD IDord-e6dd642600d64666b6ac13e904e2c92b
Source noteuspto-grants-2008_09