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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610752Generated: October 30, 2026

Azobisisobutyronitrile → 1-(Bromomethyl)-4-(2,2,3,3,3-pentafluoropropyl)benzene

https://huagongshe.com/reaction/1610752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant4-(2,2,3,3,3-Pentafluoropropyl)tolueneHCID 12756850—
SolventCarbon TetrachlorideHCID 5943—
Product1-(Bromomethyl)-4-(2,2,3,3,3-pentafluoropropyl)benzeneHCID 2226231231%

Reaction Steps

To a solution of 4-(2,2,3,3,3-pentafluoropropyl)toluene (9.97 g, 39.4 mmol) in carbon tetrachloride (300 ml) were added 2,2′-azobisisobutyronitrile (0.33 g, 197 mmol) and N-bromosuccinimide (8.50 g, 47.3 mmol) and the mixture was heated under reflux overnight. After cooling to room temperature, insoluble material was filtered off, and the filtrated was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:0, 50:1, 20:1) to give 1-(bromomethyl)-4-(2,2,3,3,3-pentafluoropropyl)benzene (3.66 g, 31% (yield by two steps)) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-175b33ddc9c94cd897e92ccdd0b357f4
Source noteuspto-grants-2006_01