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HRID 1974042作成日:2026年10月27日

Methyl perfluorooctanoate → 9H,9H-Triacontafluoro-8,10-heptadecanedione

https://huagongshe.com/reaction/1974042

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl perfluorooctanoateHCID 67824—
反応物IsoxazolineHCID 12304501—
反応物Methyl Pentadecafluoroheptyl KetoneHCID 12603809—
溶媒AcetoneHCID 180—
生成物9H,9H-Triacontafluoro-8,10-heptadecanedioneHCID 4983346—

反応手順

The beta-diketones which are used in carrying out this invention can be prepared by perfluoroacylation of appropriate ketones by esters or acid chlorides of perfluorocarboxylic acids, as in the reaction of methyl perfluorocaprylate with methyl tertiary butyl ketone to make 1-perfluoroheptyl-3 tertiary butyl-1,3 propanedione. Or a methyl perfluoroalkyl ketone can be acylated by an appropriate carboxylic derivative, as in the reaction of methyl phenylacetate with methyl perfluoropentyl ketone to give 1-perfluoropentyl-3-phenyl-1,3-propanedione; or in order to have two perfluorinated groups in the eventual isoxazoline, a methyl ketone containing also a perfluoroalkyl group can be acylated by an ester of a perfluorinated carboxylic acid, as when methyl perfluorocaprylate is reacted with methyl perfluoroheptyl ketone to produce 1,3-di(perfluoroheptyl)-1,3-propanedione.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04000150
出典データセットuspto-grants-1976_12
ORD IDord-e1035c1bbaf246e09eec645270a5a387
出典メモuspto-grants-1976_12