Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl 4-phenyl-3,6-dihydropyridine-1(2H)-carboxylate | HCID 15442738 | — |
| Catalyst | Potassium ferricyanide | HCID 26250 | — |
| Catalyst | 1,4-Bis(dihydroquinidine)phthalazine | HCID 11217202 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 59808495 | HCID 59808495 | — |
Reaction Steps
To a solution of potassium osmate (VI) 2 hydrate (8.0 g), (DHQD)2PHAL (14.2 g), potassium carbonate (379 g), potassium hexacyanoferrate (III) (903 g) in t-butanol (4.8 L) and water (4.8 L) was added methenesulfonamide (73.4 g) at room temperature. Then, tert-butyl 4-phenyl-3,6-dihydropyridine-1(2H)-carboxylate (200 g) was added thereto in an ice-bath, and the mixture was stirred for 2 hours. The mixture was further stirred at room temperature for 12 hours, and thereto was added methylene chloride (7.0 L) for separation to give the organic layer. The aqueous layer was washed twice with methylene chloride, and the obtained organic layers were combined, washed with 2M aqueous potassium hydroxide solution, dried over anhydrous sodium sulfate, and the solvent was removed by evaporation under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1) to give the title compound (215.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389511B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-4797e5e7d8f54dda9945dfbe1f2bfe92 |
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| Source note | uspto-grants-2013_03 |
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