HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875138Generated: October 31, 2026
Azobisisobutyronitrile → 3-{[3-(Bromomethyl)-6-chloro-2-fluorophenyl]oxy}-5-(trifluoromethyl)benzonitrile
https://huagongshe.com/reaction/1875138
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-[(6-Chloro-2-fluoro-3-methylphenyl)oxy]-5-(trifluoromethyl)benzonitrile | HCID 68487404 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-{[3-(Bromomethyl)-6-chloro-2-fluorophenyl]oxy}-5-(trifluoromethyl)benzonitrile | HCID 86644938 | 49% |
Reaction Steps
To a solution of 3-[(6-chloro-2-fluoro-3-methylphenyl)oxy]-5-(trifluoromethyl)benzonitrile (12.2 g, 37.0 mmol) and N-bromosuccinimide (6.59 g, 37.0 mmol) in carbon tetrachloride (300 mL) was added AIBN (0.304 g, 1.850 mmol) and the mixture was stirred at 75° C. for 4 hours. More AIBN (0.304 g, 1.850 mmol) was added and the reaction mixture was stirred overnight at 75° C. The mixture was filtered through a pad of Celite and the filtrate was concentrated. The crude oil was purified via silica gel chromatography to give 3-{[3-(bromomethyl)-6-chloro-2-fluorophenyl]oxy}-5-(trifluoromethyl)benzonitrile (7.33 g, 17.94 mmol, 49% yield). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.63 (s, 1H), 7.42 (s, 1H), 7.31-7.36 (m, 2H), 7.24 (d, 1H), 4.48 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-2c2d2d062eee45d88717875f88de11fe |
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| Source note | uspto-grants-2012_11 |
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