HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533496Generated: October 30, 2026
Benzoyl Peroxide → 4-(Bromomethyl)benzophenone
https://huagongshe.com/reaction/533496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 4-Methylbenzophenone | HCID 8652 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(Bromomethyl)benzophenone | HCID 122951 | — |
Reaction Steps
4-Methyl benzophenone (product of Aldrich) (25.1 parts), N-bromo succinimide [product of Wako Pure Chemical industries, Ltd.] (22.8 parts), benzoyl peroxide [water content: 20%, product of Wako Pure Chemical Industries, Ltd.] (0.54 parts), and acetonitrile (80 parts) were mixed, heated to 80° C., and allowed to react for 2 hours under reflux. Subsequently, the resulting mixture was cooled, and the organic solvent was evaporated under reduced pressure. The residue was recrystallized in methanol (160 parts). As a result, 26 parts of an intermediate (C123-6-1) was obtained (as white crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853290B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-a4649a9d08a34b50af0abca997f24276 |
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| Source note | uspto-grants-2014_10 |
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