Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050048Generated: November 2, 2026

Azobisisobutyronitrile → HCID 20343345, compound

https://huagongshe.com/reaction/2050048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 20343346HCID 20343346—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 20343345HCID 2034334551%

Reaction Conditions

Temperature10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04199596
Source datasetuspto-grants-1980_04
ORD IDord-38f63836358e4099a5103ff96aad8410
Source noteuspto-grants-1980_04