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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422915Generated: October 30, 2026

Triacetoxyperiodinane → HCID 86596703, compound

https://huagongshe.com/reaction/422915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 66673009HCID 66673009—
SolventDichloromethaneHCID 6344—
ProductHCID 86596703HCID 8659670397%

Reaction Steps

To a solution of (2R)-2-t-butoxycarbonylamino-2-methyl-4-[5-(5-phenylpentanoyl)furan-2-yl]butan-1-ol (110.2 mg, 0.26 mmol) obtained in Example (29a) in dichloromethane (2.6 ml) was added Dess-Martin reagent (165.0 mg, 2.28 mmol), and the resulting mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour. After stirring, the reaction mixture was evaporated in vacuo, and to the residue was added a 10% aqueous sodium thiosulfate solution to decompose the excess reagent. The resulting mixture was extracted with dichloromethane, and the extract was washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. After filtration, the solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of hexane and ethyl acetate (3:1) as the eluent to afford the title compound (105.9 mg, yield: 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101650B2
Source datasetuspto-grants-2012_01
ORD IDord-fe8f2b3a30aa4de8a3a4deb1050bde5e
Source noteuspto-grants-2012_01