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HRID 443448作成日:2026年10月25日

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

https://huagongshe.com/reaction/443448

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物N-bromobutanimideHCID 67184—
反応物Methyl (3-(trifluoromethyl)phenyl)acetateHCID 2734603—
触媒TriethylamineHCID 8471—
溶媒Carbon TetrachlorideHCID 5943—
生成物Methyl 2-bromo-2-[3-(trifluoromethyl)phenyl]acetateHCID 19796654—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04260620
出典データセットuspto-grants-1981_04
ORD IDord-0ef1a9bcd15e49589cf3dd7213991fb6
出典メモuspto-grants-1981_04