戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 439673作成日:2026年10月23日

Isopropanol → 4-Bromo-3-chloro-3,4,4-trifluorobutanoic acid

https://huagongshe.com/ja/reaction/439673

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物4-Bromo-3-chloro-3,4,4-trifluorobutan-1-olHCID 21836477—
反応物Jones' reagentHCID 131709961—
溶媒AcetoneHCID 180—
溶媒DichloromethaneHCID 6344—
生成物4-Bromo-3-chloro-3,4,4-trifluorobutanoic acidHCID 1091212785%

反応手順

A solution of 4-bromo-3-chloro-3,4,4-trifluorobutanol (IX) (2.41 g, 10 mmol) in acetone (35 mL) was treated with Jones reagent (7.5 mL) in 10 min with stirring and cooling (ice-water bath). The mixture was then stirred at room temperature for 30 min and 0.5 mL of i-propanol was then added. The precipitated salts were removed by filtration, washed with acetone. The residue obtained after concentration of the filtrate was dissolved in methylene chloride (100 mL), washed with 1N HCl (50 mL), brine, and dried over anhydrous magnesium sulfate. Evaporation of the solvent gave 2.17 g (85%) of 4-bromo-3-chloro-3,4,4-trifluorobutanoic acid (VIII) as a clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05514717
出典データセットuspto-grants-1996_05
ORD IDord-77eaa78347e14d699c10a4101f11b5b8
出典メモuspto-grants-1996_05