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HRID 567636作成日:2026年10月26日

Toluene → 13,13,13,12,12,11,11,10,10,9,9,8,8,7,7,6,6-Heptadecafluoro-3-oxatridecanoic acid-t-butyl ester

https://huagongshe.com/reaction/567636

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物1,1,2,2-Tetrahydroperfluoro-1-decanolHCID 69619—
反応物tert-Butyl bromoacetateHCID 79177—
触媒Tetrabutylammonium hydrogen sulfateHCID 94433—
溶媒Potassium HydroxideHCID 14797—
生成物13,13,13,12,12,11,11,10,10,9,9,8,8,7,7,6,6-Heptadecafluoro-3-oxatridecanoic acid-t-butyl esterHCID 22352715—

反応条件

温度0 °C

反応手順

10.51 g (53.9 mmol) of bromoacetic acid-tert-butyl ester is added in drops to a mixture of 10 g (21.55 mmol) of 1H,1H,2H,2H-perfluorodecan-1-ol and 0.73 g (2.15 mmol) of tetrabutylammonium hydrogen sulfate in 100 ml of 60% potassium hydroxide solution/50 ml of toluene while being stirred vigorously at 0° C. It is stirred for 1 hour at 0° C. 200 ml of toluene is added, the aqueous phase is separated and extracted twice with 50 ml of toluene each. The combined organic phases are dried on magnesium sulfate and concentrated by evaporation in a vacuum. The residue is chromatographed on silica gel (mobile solvent: hexane/dichlormethane/acetone=20/10/1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06180113B2
出典データセットuspto-grants-2001_01
ORD IDord-31ecd48878a447e99291e5f76dbbc009
出典メモuspto-grants-2001_01