Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289320Generated: October 30, 2026

Azobisisobutyronitrile → HCID 18700114, compound

https://huagongshe.com/reaction/2289320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactantalpha,alpha,beta,beta-Tetrafluoro-2-methylphenetoleHCID 2776650—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 18700114HCID 18700114—

Reaction Steps

To a stirred solution of 2-(1,1,2,2-tetrafluoroethoxy)toluene (2.5 g, 12.2 mmol) in CCl4 (75 mL) was added NBS (2.1 g, 13 mmol) and AIBN (0.65 g, 3 mmol). The mixture was refluxed for 6 h. The solvent was removed under reduced pressure and the residue was partitioned between EtOAc (75 mL) and water (50 mL). The organic phase was separated, dried (MgSO4), filtered, and the solvent was removed under reduced pressure. The residue was purified by pressurized silica gel column chromatography using hexanes as eluant to give 2-(1,1,2,2-tetrafluoroethoxy)benzyl bromide as a colorless liquid (TLC Rf =0.7 (hexanes)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090805
Source datasetuspto-grants-2000_07
ORD IDord-ab0076abff254452b73db0515c85e17e
Source noteuspto-grants-2000_07