戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1702859作成日:2026年10月26日

Water → 2,3,3,3-Tetrafluoro-2-(1,1,2,3,3,3-hexafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy)propoxy)propanoic acid

https://huagongshe.com/reaction/1702859

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Hexafluoropropene oxide trimerHCID 102863—
反応物Potassium FluorideHCID 522689—
反応物HCID 178477749HCID 178477749—
溶媒DiglymeHCID 8150—
生成物2,3,3,3-Tetrafluoro-2-(1,1,2,3,3,3-hexafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy)propoxy)propanoic acidHCID 93076—

反応手順

A suspension of 58.1 g (1.0 mol) of flame-dried KF in 1400 ml of dry diglyme was stirred at 25° while 333 g (0.67 mol) of hexafluoropropene oxide trimer was added rapidly. The two-phase system was stirred at 25° for 2 hr, during which time about half of the fluorocarbon layer slowly dissolved. The mixture was stirred at 5°-10° while 230 g (1.0 mol) of 1 was added. The mixture was stirred at 5°-10° for 2.5 hr, then overnight at 25°, and poured into 2 l. of H2O. The aqueous layer was extracted with 100 ml of CFCl2CF2Cl, and the combined organic layers washed with 2 l. of H2O, extracted with 100 ml of conc. H2SO4, clarified with CaSO4, filtered and distilled. Hydrolysis and bubbling were apparent in the water washed. Distillation afforded major fractions of 2 and 3, bp 55°-71° (20 mm) and 140 g of crude CF3CF2CF2OCF(CF3)CF2OCF(CF3)CO2H, bp mainly 101°-104° (20 mm). Redistillation of combined fractions of 2 and 3 gave 80 g of impure 3, bp 81°-86° (80 mm) and 33.0 g (8%) of 2, bp 94°-95° (80 mm).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04349650
出典データセットuspto-grants-1982_09
ORD IDord-f588b85fcda643b381cd6d33a56cf6fd
出典メモuspto-grants-1982_09