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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625708Generated: October 28, 2026

2'-Aminoacetophenone → 1-(2-Amino-5-bromophenyl)ethan-1-one

https://huagongshe.com/reaction/1625708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2'-AminoacetophenoneHCID 11086—
ReactantN-bromobutanimideHCID 67184—
SolventDichloromethaneHCID 6344—
Product1-(2-Amino-5-bromophenyl)ethan-1-oneHCID 11074746—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A flask charged with 1-(2-aminophenyl)ethanone (135 mg) and DCM (2.5 mL) was cooled to −10° C. and NBS (178 mg) was added in several portions over 30 min. The reaction mixture was diluted with 10 mL DCM, washed with sat. aqueous NaHCO3, dried over Na2SO4, filtered and concentrated under reduced pressure, affording the title compound. MS (ESI+): m/z 215.06 (MH+). 1H NMR (400 MHz, CDCl3): δ 7.79 (s, 1H), 7.31 (d, J=8.8 Hz, 1H), 6.54 (d, J=8.8 Hz, 1H), 6.30 (br, 2H), 2.55 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785151B2
Source datasetuspto-grants-2014_07
ORD IDord-fd67351b5bdc45bcaffb36285ab5fceb
Source noteuspto-grants-2014_07