Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydroxide | HCID 961 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 131724702 | HCID 131724702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178506956 | HCID 178506956 | — |
Reaction Steps
FSO2(CF2)4OCH2C6H5 was treated with excess aqueous lithium hydroxide as described in Preparation of Precursor 3 except that the solution was heated at 75° C. for eighteen hours. After neutralization of the excess hydroxide with solid carbon dioxide, it was noted that a lower fluorochemical-containing phase was still present. Additional lithium hydroxide was added as well as about 50 mL of methanol and the reaction mixture heated to 84° C. for an additional eighteen hours. This solution was then neutralized in the usual manner and LiO3S(CF2)4OCH2C6H5 was isolated after alcohol extraction (9.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06841333B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-96c3c70a87364f768e7319f3b6f20a86 |
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| Source note | uspto-grants-2005_01 |
|---|