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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942509Generated: November 3, 2026

Water → HCID 59808495, compound

https://huagongshe.com/reaction/1942509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-phenyl-3,6-dihydropyridine-1(2H)-carboxylateHCID 15442738—
CatalystPotassium ferricyanideHCID 26250—
Catalyst1,4-Bis(dihydroquinidine)phthalazineHCID 11217202—
Solventtert-ButanolHCID 6386—
ProductHCID 59808495HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389511B2
Source datasetuspto-grants-2013_03
ORD IDord-4797e5e7d8f54dda9945dfbe1f2bfe92
Source noteuspto-grants-2013_03