Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 2-Methyl-2-butene | HCID 10553 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | HCID 86731312 | HCID 86731312 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86731313 | HCID 86731313 | — |
Reaction Steps
To a mixture of 4-fluoro-5-(methoxymethoxy)pyridine-2-carbaldehyde (2.43 g), sodium dihydrogen phosphate (4.72 g), 2-methyl-2-butene (7.32 mL), water (4 mL) and tert-butanol (20 mL) was added sodium chlorite (2.23 g), and the mixture was stirred at room temperature for 2.5 hr. The reaction mixture was acidified with 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was dissolved in DMF (30 mL), potassium carbonate (1.81 g) and methyl iodide (0.820 mL) were added thereto, and the mixture was stirred at 70° C. for 20 min. To the reaction mixture was added water, and the obtained mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (1.80 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09133129B2 |
|---|
| Source dataset | uspto-grants-2015_09 |
|---|
| ORD ID | ord-c8ca71e40a7b446a84bf469b5e9fe2bc |
|---|
| Source note | uspto-grants-2015_09 |
|---|