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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194518Generated: October 31, 2026

p-Toluenesulfonic acid → (3'aR,6'aS)-hexahydro-1'H-spiro(1,3-dioxolane-2,2'-pentalen)-5'-one

https://huagongshe.com/reaction/1194518

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium BicarbonateHCID 516892—
ReactantPropan-2-one--water (1/1)HCID 18366337—
Product(3'aR,6'aS)-hexahydro-1'H-spiro(1,3-dioxolane-2,2'-pentalen)-5'-oneHCID 11030443—

Reaction Steps

A mixture of 53.9 g of 3,3,7,7-diethylenedioxy-cis-bicyclo[3.3.0]octane as prepared in Referential Example 1, 2.26 g of p-toluenesulfonic acid and 500 ml of acetone-water (3:1) was stirred at room temperature for 1 hour and 40 minutes. Then, to the mixture was added 50 ml of saturated aqueous sodium hydrogencarbonate solution, the deposited crystals was filtered off and acetone was removed in vacuo from the filtrate, and the residue was extracted with chloroform. The organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated. To the residue was added to 50 ml of a mixture of n-hexane/diethyl ether (1:1) and then crystals were deposited. After separating out the crystals by filtration, the filtrate was concentrated, and the residue was purified by silica gel chromatography (eluting solution: 20-30% (v/v) ethyl acetate/n-hexane) to obtain 20.4 g of the oily title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04814468
Source datasetuspto-grants-1989_03
ORD IDord-9d62038ecaf14d6fbe19f668d497fc55
Source noteuspto-grants-1989_03