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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395203Generated: October 26, 2026

Azobisisobutyronitrile → Methyl 2-bromo-2-[3-(trifluoromethyl)phenyl]acetate

https://huagongshe.com/reaction/1395203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl (3-(trifluoromethyl)phenyl)acetateHCID 2734603—
CatalystTriethylamineHCID 8471—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 2-bromo-2-[3-(trifluoromethyl)phenyl]acetateHCID 19796654—

Reaction Steps

To the solution of 21.8 g of methyl m-trifluoromethylphenylacetate in 450 ml of carbon tetrachloride a portion of 18.7 g of N-bromosuccinimide is added along with several drops of triethylamine and a pinch of azobisisobutyronitrile. The mixture is warmed to reflux with a 250 watt incandescent bulb and a precipitate is formed. Thereupon the remainder of N-bromosuccinimide is added, the light removed and the solution stirred for 3 hours. It is cooled in an ice bath and the solid formed removed by filtration. The filtrate is evaporated the residue dissolved in diethyl ether-water and the organic phase washed with aqueous sodium bicarbonate and water. It is dried, evaporated, the residue distilled and the fraction boiling at 85°-88°/0.4 mmHg collected, to yield the methyl α-bromo-m-trifluoromethylphenylacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04202901
Source datasetuspto-grants-1980_05
ORD IDord-25fba002a98342d2b24f3af449f3b392
Source noteuspto-grants-1980_05