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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl perfluorooctanoate | HCID 67824 | — |
| Reactant | Isoxazoline | HCID 12304501 | — |
| Reactant | Methyl Pentadecafluoroheptyl Ketone | HCID 12603809 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 9H,9H-Triacontafluoro-8,10-heptadecanedione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04000150 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-e1035c1bbaf246e09eec645270a5a387 |
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| Source note | uspto-grants-1976_12 |
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