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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662941Generated: October 25, 2026

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

https://huagongshe.com/reaction/1662941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanone, 1-(5-amino-2-nitrophenyl)-HCID 6420386—
ReactantHydrobromide monohydrateHCID 22326455—
ReactantSodium NitriteHCID 23668193—
Product1-(5-Bromo-2-nitrophenyl)ethanoneHCID 12224157—

Reaction Conditions

Temperature60 °C

Reaction Steps

In the ice bath, the starting material, about 10 mmol of 3-acetyl-4-nitro-aminobenzene was added into HBr/H2O (about 100 mL, 1/2, v/v), and sodium nitrite solution was gradually added. The solution was stirred at about 60° C. for about 2 hours. After the reaction was completed, the precipitate was filtered. The filtered solution was neutralized with about 1N NaOH, and extracted with EtOAc. Then the extracted material was dried with sodium sulfate anhydride. Next, the dried material was distilled under reduced pressure. Then, 3-acetyl-4-nitro-bromobenzene was obtained in a form of about 75% yellow oil using silica gel column chromatography (Hexane/EtOAc=2/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034747B2
Source datasetuspto-grants-2011_10
ORD IDord-2584ff91657842e0ab26364f0533adf3
Source noteuspto-grants-2011_10