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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755657Generated: November 1, 2026

Azobisisobutyronitrile → Methyl 2-(1-bromoethyl)benzoate

https://huagongshe.com/reaction/1755657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-ethylbenzoateHCID 583295—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 2-(1-bromoethyl)benzoateHCID 1587065482.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

N-Bromosuccinimide (10.7 g) and azodiisobutyronitrile (catalytic) were added to a solution of methyl 2-ethylbenzoate (10 g) in carbon tetrachloride (50 ml), and the resulting mixture was heated at 80° C. for 6 hours under reflux. After cooling, the reaction mixture was filtered and the filtrate was concentrated to give methyl 2-(1-bromoethyl)benzoate (12 g), almost pure by GC and NMR, as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438059
Source datasetuspto-grants-1995_08
ORD IDord-697f9014e60f4b3b8ba4cb324ae45826
Source noteuspto-grants-1995_08