HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538620Generated: October 26, 2026
Azobisisobutyronitrile → 7-(Bromomethyl)quinoline
https://huagongshe.com/reaction/538620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 7-Methylquinoline | HCID 11927 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 7-(Bromomethyl)quinoline | HCID 14168508 | 58% |
Reaction Steps
To a solution of 7-methylquinoline (0.10 g, 0.70 mmol) in 5 ml of CCl4 was added NBS (0.14 g, 0.77 mmol) and AIBN (0.025 g, 0.15 mmol). The reaction mixture was heated at 100° C. for 2 h under nitrogen atmosphere. After the completion of the reaction mixture (TLC monitoring), the reaction mixture was evaporated to dryness under reduced pressure and the residue was purified by column chromatography on silica (230-400M) using 1% ethyl acetate/hexane eluent to give the desired product (0.090 g, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865736B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-66ded7ddc0234daaae4ba99bfa3da2c4 |
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| Source note | uspto-grants-2014_10 |
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