HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658508Generated: November 2, 2026
Benzoyl Peroxide → 3',4'-Dichloro-2-fluoro-4-bromomethyl-biphenyl
https://huagongshe.com/reaction/658508
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3',4'-Dichloro-2-fluoro-4-methyl-biphenyl | HCID 66916736 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3',4'-Dichloro-2-fluoro-4-bromomethyl-biphenyl | HCID 66916717 | — |
Reaction Steps
3′,4′-dichloro-2-fluoro-4-methyl-biphenyl (29 g, 0.114 mol), N-bromosuccinimide (21.2 g, 0.119 mol), benzoyl peroxide (1.4 g, 0.004 mol) were dissolved in acetonitrile (190 ml). The mixture was refluxed for 3 hours, then cooled, mixed with a solution of sodium sulphite (2.2 g) in water (54 ml), stirred for 30 minutes and then allowed to rest to separate the phases. The lower aqueous phase was separated and extracted with dichloromethane (29 ml). The upper phase was concentrated under vacuum, mixed with water (10 ml), and dichloromethane (58 ml) and stirred. The organic phases were separated and put together, washed twice with water (29 ml), and concentrated under vacuum. The compound 3′,4′-dichloro-2-fluoro-4-bromomethyl-biphenyl was isolated as an orange oil (35.7 g, 94% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076505B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-04476d7e230b45209aca6cae7e8145c6 |
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| Source note | uspto-grants-2011_12 |
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