Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Phosphate, Monobasic, Monohydrate | HCID 516949 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | HCID 86659062 | HCID 86659062 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 66990671 | HCID 66990671 | 122.5% |
Reaction Steps
To a stirred solution of the compound prepared in Example 423 (1.66 g) in dioxane (40 mL) at room temperature was added 2-methyl-2-butene (2.0 mol/L; 25.811 mL) in tetrahydrofuran. To the resulting stirred solution was added a solution of sodium chlorite (4.2095 g) and sodium phosphate monobasic monohydrate (4.2039 g) in water (28 mL). The resulting two-phase mixture was vigorously stirred at room temperature. The color of the reaction mixture lightened considerably over the first 30 minutes. After 18 hours, the reaction mixture was diluted with ethyl acetate (50 mL) and transferred to a separatory funnel. The aqueous layer was acidified with concentrated hydrochloric acid to about pH 1.5, and the resulting mixture was extracted with ethyl acetate. The organic layer was dried, evaporated and dried further under high vacuo to provide the title compound (2.2 g) as a pale orange oil with the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809538B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-2b6942d697ed480697a0cdb3402b41b3 |
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| Source note | uspto-grants-2014_08 |
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