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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681516Generated: November 4, 2026

4-(5-Hydroxy-3-hexadecynyl)-2-triethylsilylfuran → 4-(5-Oxo-3-hexadecynyl)-2-triethylsilylfuran

https://huagongshe.com/reaction/1681516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(5-Hydroxy-3-hexadecynyl)-2-triethylsilylfuranHCID 15037106—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventSulfuric AcidHCID 1118—
Product4-(5-Oxo-3-hexadecynyl)-2-triethylsilylfuranHCID 15037107—

Reaction Steps

Jones reagent (a 2.6M solution in sulfuric acid; 0.13 ml, 0.36 mmol) was added dropwise to a solution of 4-(5-hydroxy-3-hexadecynyl)-2-triethylsilylfuran (136.4 mg, 0.33 mmol) in acetone (5 ml) at 0 degrees. After 20 minutes, the excess Jones reagent was destroyed with ethanol (ca 1 ml) and the mixture was diluted with water. The organic phase was separated, dried (magnesium sulfate) and evaporated down to give an oil, which was purified by preparative silica plates to give the titled ketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05171863
Source datasetuspto-grants-1992_12
ORD IDord-4eb508bac72a47efbfac319d98972069
Source noteuspto-grants-1992_12