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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396645Generated: October 30, 2026

Ethyl vinyl ether → HCID 19046364, compound

https://huagongshe.com/reaction/2396645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl vinyl etherHCID 8023—
ReactantHCID 19046422HCID 19046422—
ReactantLithium perchlorateHCID 23665649—
SolventDiethyl EtherHCID 3283—
SolventSodium BicarbonateHCID 516892—
ProductHCID 19046364HCID 19046364—

Reaction Steps

To a solution of 3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxy-5-isobenzofurnylmethyl)-2-methylcyclopent-2-en-1-ol (0.157 g) in ethyl vinyl ether (10 mL) was added mercuric acetate (0.052 g). After stirring for 30 hours at ambient temperature, the reaction was diluted with ether and passed quickly through a fritted funnel half filled with celite and capped with silica. To this ethereal solution [containing 3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxy-5-isobenzofuranylmethyl)-2-methyl-1-vinyloxycyclopent-2-ene, which was not isolated or characterized] was then added lithium perchlorate (10 mL, 0.5M solution in ether). After 0.5 hours, the reaction was diluted with aqueous sodium bicarbonate and washed with brine. Drying over magnesium sulfate was followed by filtration and solvent removal. The product 3-(1,3-dihydro-6-methoxy-7-methyl-3-oxo-4-p-toluenesulfonyloxy-5-isobenzofuranylmethyl)-2-methylcyclopent-2-en-1-ylacetaldehyde (0.050 g) was finally obtained after chromatography (hexanes/ethyl acetate, 2/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05493030
Source datasetuspto-grants-1996_02
ORD IDord-6c58e5ea89a04c5f8479bd2bf2f5aa95
Source noteuspto-grants-1996_02