HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572549Generated: October 29, 2026
Azobisisobutyronitrile → 3-(Bromomethyl)-5-fluorobenzonitrile
https://huagongshe.com/reaction/572549
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Fluoro-5-methylbenzonitrile | HCID 2778446 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(Bromomethyl)-5-fluorobenzonitrile | HCID 66652629 | — |
Reaction Steps
3-Fluoro-5-methylbenzonitrile (Hognda Trading; 100 g, 0.74 mol) was taken in acetonitrile (1 L) at 25° C. under nitrogen atmosphere. N-Bromosuccinimide (105 g, 0.59 mol) and AIBN (2.4 g, 0.014 mol) were added and the reaction mixture was heated at 70° C. for 1 h 20 minutes. The reaction mixture was cooled to 25° C. and concentrated. The residue was diluted, cooled to 0-5° C. and stirred for 15 minutes at the same temperature. The precipitated succinimide was filtered and the filtrate was concentrated to get crude product as yellow oil (90 g). It was taken in petroleum ether (200 mL) and cooled to −20° C. stirred for 30 minutes. The precipitated solids were filtered and dried to get the title product as white solid. 1H NMR (DMSO-d6; 400 MHz): δ 7.83 (m, 2H), 7.73 (m, 1H), 4.72 (s, 2H). HPLC (Method A) Rt: 4.17 min (Purity: 99.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029405B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-f45ca2caf7854056af437cc9a310816c |
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| Source note | uspto-grants-2015_05 |
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