HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425039Generated: October 29, 2026
Azobisisobutyronitrile → HCID 59557730, compound
https://huagongshe.com/reaction/425039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 23560508 | HCID 23560508 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 59557730 | HCID 59557730 | — |
Reaction Steps
To a solution of (5-bromo-2-chlorophenyl)(p-tolyl)methanone (intermediate AG) (16 g, 48.9 mmol) in CCl4 (80 mL), NBS (10.08 g, 57 mmol) and AIBN (0.848 g) was added. Then the mixture was heated to 90° C. After 3 h, CCl4 was removed under reduced pressure. The residue was dissolved in CH2Cl2 and the solution was washed 1× with HCl (1M) and 2× with brine prior to drying over Na2SO4. Solvent was removed under reduced pressure to obtain crude intermediate AH (20.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106021B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-5353343df86c44debcb2a256a4604e10 |
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| Source note | uspto-grants-2012_01 |
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