Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 2,6-Di-tert-butylhydroquinone | HCID 75550 | — |
| Reactant | HCID 21542859 | HCID 21542859 | — |
| Product | HCID 86733317 | HCID 86733317 | — |
Reaction Steps
The compounds of this invention may be prepared according to the method of E. J. Bourne, M. Stacey, J. C. Tetlow, and J. M. Tedder (J. Chem. Soc. 1949 2976) in which one equivalent of a 2,6-di tert.alkyl hydroquinone, such as 2,6-di tert.butyl hydroquinone and 2,6-di tert. 1,3-dimethylbutyl hydroquinone, is reacted with a mixture of 1 to 1.5 equivalents of an α,β-unsaturated organic acid, acrylic acid or methacrylic acid, and 1 to 1.5 equivalents of trifluoroacetic acid anhydride or a mixture of 1 to 1.5 equivalents of an α,β-unsaturated organic acid anhydride such as maleic anhydride and 1 to 1.5 equivalents of trifluoracetic acid. The reaction temperature may vary from room temperature to about 60° C. and the time required to complete the reaction may vary from about 30 minutes to about 12 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03953402 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-a54c95ff99c44194a2b0bbfdccfdbb99 |
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| Source note | uspto-grants-1976_04 |
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