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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 443448Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/443448

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
EduktN-bromobutanimideHCID 67184—
EduktMethyl (3-(trifluoromethyl)phenyl)acetateHCID 2734603—
KatalysatorTriethylamineHCID 8471—
LösungsmittelCarbon TetrachlorideHCID 5943—
ProduktMethyl 2-bromo-2-[3-(trifluoromethyl)phenyl]acetateHCID 19796654—

Reaktionsschritte

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 reminder 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04260620
Quelldatensatzuspto-grants-1981_04
ORD IDord-0ef1a9bcd15e49589cf3dd7213991fb6
Quellennotizuspto-grants-1981_04