HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433010Generated: October 28, 2026
Bromine → 2-bromo-2-(4-fluoro-phenyl)-1-(3-isopropyl-3H-benzotriazol-5-yl)-ethanone
https://huagongshe.com/reaction/433010
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-(4-Fluoro-phenyl)-1-(3-isopropyl-3h-benzotriazol-5-yl)-ethanone | HCID 18760801 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-bromo-2-(4-fluoro-phenyl)-1-(3-isopropyl-3H-benzotriazol-5-yl)-ethanone | HCID 18760789 | — |
Reaction Steps
To a stirred solution of 191 mg of 2-(4-fluoro-phenyl)-1-(3-isopropyl-3H-benzotriazol-5-yl)-ethanone in 2 mL of acetic acid was added 0.64 mL of bromine (1 M in acetic acid). The mixture was heated at 50° C. for 3 hours. The reaction mixture was cooled to 22° C. and concentrated to dryness. The residue was taken-up into ethyl acetate and washed with saturated aqueous sodium bicarbonate, brine; the organic layer was dried (sodium sulfate), filtered and the filtrate was concentrated to give 222 mg of 2-bromo-2-(4-fluoro-phenyl)-1-(3-isopropyl-3H-benzotriazol-5-yl)-ethanone as a light yellow oil. This material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06664395B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-4f30ae2800604409954b23b94c2854d5 |
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| Source note | uspto-grants-2003_12 |
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