Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 58419191 | HCID 58419191 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58419187 | HCID 58419187 | — |
Reaction Steps
Dimethyl 2-(1,1,2-trifluoro-2-(1,1,2,3,3,3-hexafluoro-2-(perfluoropropoxy)-propoxy)ethoxy)terephthalate as prepared in Example 11 (2.25 g, 0.035 mol) was added to a solution of water (50 mL) and potassium hydroxide (KOH, 1.96 g) in a reaction flask. The resulting solution in the reaction flask was heated for 5 hours, cooled to room temperature (about 25° C.) and then acidified by adding concentrated HCl to the reaction flask until a pH of ˜1 was achieved, determined by the formation of a precipitate in the reaction flask. The resulting precipitate was filtered and dried under vacuum. Proton NMR of this precipitate showed the desired material, 2-(1,1,2-trifluoro-2-(1,1,2,3,3,3-hexafluoro-2-(perfluoropropoxy)propoxy)ethoxy)terephthalic acid. The precipitate was then crystallized from ethyl acetate (EtOAc, ˜1 part) and hexane (˜4 parts). After filtration and drying under vacuum, the resulting white di-acid, 2-(1,1,2-trifluoro-2-(1,1,2,3,3,3-hexafluoro-2-(perfluoropropoxy)propoxy)ethoxy)terephthalic acid, had a melting point of 236-239° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08350099B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-f37a82a3a40f44dbb243e78454d202ab |
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| Source note | uspto-grants-2013_01 |
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