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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711387Generated: October 26, 2026

N-(2-Acetylphenyl)acetamide → N-(2-acetyl-4-bromophenyl)acetamide

https://huagongshe.com/reaction/711387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Acetylphenyl)acetamideHCID 21306—
ReactantBromineHCID 24408—
SolventAcetic AcidHCID 176—
ProductN-(2-acetyl-4-bromophenyl)acetamideHCID 45929186.5%

Reaction Steps

Under N2, a pale yellow suspension of crude N-(2-acetylphenyl)acetamide (28 g, 158 mmol) in AcOH (300 mL) was stirred for about 5 min, and Br2 (12.95 mL, 253 mmol) was added within 1 h at room temperature. The resulting mixture was then stirred at room temperature for 75 min. After the reaction went to completion as monitored by LC-MS, the reaction mixture was quenched with H2O (200 mL). The mixture was filtered through Buchner funnel, and the solid was collected as N-(2-acetyl-4-bromophenyl)acetamide (35 g, yield 86%). MS (m/z): 216 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181264B2
Source datasetuspto-grants-2015_11
ORD IDord-9b630fec78ce435691e5aa86e1ea7c20
Source noteuspto-grants-2015_11