HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329571Generated: October 28, 2026
Benzoyl Peroxide → HCID 19870965, compound
https://huagongshe.com/reaction/329571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 19870964 | HCID 19870964 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 19870965 | HCID 19870965 | 87.9% |
Reaction Steps
A solution of 4.0 grams (0.013 mole) of N-(2,3-dichloro-4-methylphenyl)phthalimide, 2.3 grams (0.013 mole) of N-bromosuccinimide and 0.3 gram of benzoyl peroxide in 200 ml of carbon tetrachloride was heated under reflux for 22 hours. The cooled reaction mixture was poured into 500 ml of ethyl acetate. The solution was washed with three 100 ml portions of water. The organic layer was dried with magnesium sulfate and was filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was subjected to column chromatography on silica gel. Elution was accomplished using ethyl acetate:heptane (1:4). The appropriate fractions were combined and concentrated under reduced pressure to yield 4.4 grams of N-(4-bromomethyl-2,3-dichlorophenyl)phthalimide as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04892578 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-c7ab51c0afd34d858acc6eadf4ec78bc |
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| Source note | uspto-grants-1990_01 |
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