HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629317Generated: October 26, 2026
N-bromobutanimide → Methyl 5-bromo-2-(bromomethyl)benzoate
https://huagongshe.com/reaction/629317
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 5-bromo-2-methylbenzoate | HCID 316201 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | (Trifluoromethyl)benzene | HCID 7368 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 5-bromo-2-(bromomethyl)benzoate | HCID 12929136 | 69% |
Reaction Steps
To a solution of methyl 5-bromo-2-methylbenzoate (5.27 g) in trifluoromethylbenzene (50.0 mL) were added AIBN (0.04 g) and N-bromosuccinimide (4.50 g), and the mixture was stirred at 90° C. for 4 hr under argon atmosphere. The reaction mixture was diluted with ethyl acetate, and the mixture was washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (4.89 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315458B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-a7919ee28acd4adba6209dc2b2df2be1 |
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| Source note | uspto-grants-2016_04 |
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