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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230708Generated: October 24, 2026

Ethanone, 1-(5-amino-2-nitrophenyl)- → 1-(5-Bromo-2-nitrophenyl)ethanone

https://huagongshe.com/en/reaction/230708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanone, 1-(5-amino-2-nitrophenyl)-HCID 6420386—
ReactantHydrobromide monohydrateHCID 22326455—
ReactantSodium NitriteHCID 23668193—
Product1-(5-Bromo-2-nitrophenyl)ethanoneHCID 1222415775%

Reaction Conditions

Temperature60 °C

Reaction Steps

10 mmol of 3-acetyl-4-nitro-aminobenzene as a starting material was added to 100 mL of HBr/H2O (1/2, v/v) and a sodium nitrite solution was slowly added dropwise thereto in an ice bath. The reaction mixture was stirred at 60° C. for 2 hours. When the reaction was completed, the precipitate was filtered off. The filtrate was neutralized with 1N NaOH, extracted with EtOAc, dried over anhydrous sodium sulfate, distilled under reduced pressure and purified by silica gel column chromatography (hexane/EtOAc=2/1) to obtain the desired 3-acetyl-4-nitro-bromobenzene as a yellow oil (75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566773B2
Source datasetuspto-grants-2009_07
ORD IDord-0a65bf957c504fd4a9138c474b2d88c4
Source noteuspto-grants-2009_07