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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658359Generated: October 29, 2026

Triacetoxyperiodinane → HCID 86645108, compound

https://huagongshe.com/reaction/658359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68497201HCID 68497201—
SolventDichloromethaneHCID 6344—
ProductHCID 86645108HCID 86645108—

Reaction Steps

1,2-dihydro-6-hydroxymethyl-2-oxo-1-phenylpyridine-3-carboxylic acid ethyl ester (5.0 g, 18 mmol) was dissolved in dichloromethane (50 mL), and a DMP reagent (1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one) (8.5 g, 20 mol) was added thereto at room temperature. The mixture was allowed to react for 4 hours. The reaction mixture was poured into an aqueous sodium bicarbonate solution, and extracted with chloroform. The organic layer was washed with water, dried, and concentrated, to obtain crude 6-formyl-1-phenyl-1,2-dihydro-2-oxopyridine-3-carboxylic acid ethyl ester. This crude product was dissolved in dichloromethane (50 mL), and a DAST reagent (diethylamino sulfur trifluoride) (4.8 g, 30 mmol) was added to this solution at 5° C. under a nitrogen atmosphere. The mixture was allowed to react overnight at room temperature. The reaction mixture was poured into water, and the organic layer was washed with an aqueous sodium bicarbonate solution and water, dried, and concentrated. Thus obtained residue was purified by column chromatography (elution solvent: hexane/ethyl acetate: 4/1 to 3/2), and thus obtained solid was washed with a mixed solution of hexane/ethyl acetate=1/1, to obtain 2.29 g of a desired product (yield: 57%, two stages).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076487B2
Source datasetuspto-grants-2011_12
ORD IDord-ea75a50266c74b39a7e25a7afa2d379f
Source noteuspto-grants-2011_12