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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920808Generated: October 30, 2026

Hydrogen Bromide → HCID 58572756, compound

https://huagongshe.com/reaction/1920808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 58572760HCID 58572760—
CatalystCopper bromide (CuBr2)HCID 24611—
ProductHCID 58572756HCID 5857275661%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(2-Amino-5-fluoro-3-methoxy phenyl)ethanone (2.66 g, 14.2 mmol), which had been obtained in Reference example 5 (5b), was suspended in 10% aqueous hydrogen bromide solution (22 mL). Then, a 9% aqueous sodium nitrite solution (11 mL, 14.4 mmol) was slowly added dropwise thereto at 0° C. After stirring the mixture solution for 1 hour at 0° C., a solution in which copper bromide (I) (2.24 g, 15.7 mmol) was dissolved in 47% aqueous hydrogen bromide solution (15 mL) was added thereto, and the mixture was refluxed with heating at 110° C. for 2 hours. The reaction solution was cooled to room temperature and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (n-hexane/ethyl acetate=4/1) to give the title compound as a pale yellow solid (2.15 g, yield 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173631B2
Source datasetuspto-grants-2012_05
ORD IDord-0004a7e6815244c7af348a3c43ee20dd
Source noteuspto-grants-2012_05