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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974042Generated: October 25, 2026

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

https://huagongshe.com/reaction/1974042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl perfluorooctanoateHCID 67824—
ReactantIsoxazolineHCID 12304501—
ReactantMethyl Pentadecafluoroheptyl KetoneHCID 12603809—
SolventAcetoneHCID 180—
Product9H,9H-Triacontafluoro-8,10-heptadecanedioneHCID 4983346—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04000150
Source datasetuspto-grants-1976_12
ORD IDord-e1035c1bbaf246e09eec645270a5a387
Source noteuspto-grants-1976_12