HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050048Generated: November 2, 2026
Azobisisobutyronitrile → HCID 20343345, compound
https://huagongshe.com/reaction/2050048
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 20343346 | HCID 20343346 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 20343345 | HCID 20343345 | 51% |
Reaction Steps
48.4 g (0.22 mol) of 3-(3-fluorophenoxy)-6-fluorotoluene were dissolved in 300 ml of anhydrous carbon tetrachloride and heated under reflux with 41 g of N-bromosuccinimide. After 70° C. was reached, 3 g of azo-diisobutyronitrile were added; after about 10-20 minutes the reaction commenced, with evolution of heat, and after the exothermic reaction had subsided the mixture was heated under reflux for a further 4 hours. The reaction batch was then cooled to 10° C., the succinimide was filtered off and the carbon tetrachloride was distilled off in vacuo. The oil which remained was distilled at 142°-150° C./2 mm Hg. 3-(3-Fluorophenoxy)-6-fluorobenzyl bromide was obtained in 51% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04199596 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-38f63836358e4099a5103ff96aad8410 |
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| Source note | uspto-grants-1980_04 |
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