HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018074Generated: October 25, 2026
N-bromobutanimide → (4-(Bromomethyl)phenyl)(cyclopropyl)methanone
https://huagongshe.com/reaction/1018074
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Chloro-4'-isopropylbutyrophenone | HCID 98744 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-(Bromomethyl)phenyl)(cyclopropyl)methanone | HCID 15512829 | 165.6% |
Reaction Steps
Dissolve 4-chloro-1-(4-isopropyl-phenyl)-butan-1-one (20 g, 124 mmol) and 2,2′-Azolons (2-methylpropionitrile) (0.5 g) in methylene chloride (100 mL) and cool to 5° C. Add a suspension of N-bromosuccinimide (12 g) in methylene chloride (50 mL) and irradiate with light (150 Watt lamp), maintaining the temperature at 5° C. After 2, 3 and 7 hour time periods, add additional N-bromosuccinimide (6 g, 6 g, 2.8 g) and continue stirring. After 7.5 hours, wash with water (200 mL) and with 0.4M sodium hydrogen carbonate (2×200 mL). Dry (Na2SO4), evaporate the solvent in vacuo and recrystallize (hexane) to give the title compound as a crystalline solid (26.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479663B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-4e301e4710e4423f9fb1f82a2cd95c6d |
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| Source note | uspto-grants-2002_11 |
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