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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2'-Aminoacetophenone | HCID 11086 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Amino-5-bromophenyl)ethan-1-one | HCID 11074746 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785151B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-fd67351b5bdc45bcaffb36285ab5fceb |
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| Source note | uspto-grants-2014_07 |
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