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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358311Generated: October 30, 2026

Acetone → HCID 67321086, compound

https://huagongshe.com/reaction/358311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBoron trifluorideHCID 6356—
ReactantDiglycidyl etherHCID 16704—
ReactantSodium BicarbonateHCID 516892—
ReactantOxirane, 2-[[(9Z)-9-octadecen-1-yloxy]methyl]-HCID 6435878—
SolventDiethyl EtherHCID 3283—
ProductHCID 67321086HCID 6732108690%

Reaction Steps

Into a round bottom flask having a capacity of 500 ml and equipped with a reflux condenser, a thermometer, a dropping funnel, a nitrogen gas supply tube, and a stirring means, 81.2 g (1.4 moles) of acetone, and 2.0 g (0.014 mole) of boron trifluoride etharate were charged and stirred while supplying a nitrogen gas. Then, 64.9 g (0.2 mole) of oleyl glycidyl ether was gradually added dropwise while supplying a nitrogen gas. The reaction mixture generates heat as the glycidyl ether is added. Therefore, the reaction mixture was cooled to maintain a temperature of from 20° to 30° C., and it took about one hour for the addition of the glycidyl ether. The stirring was continued for further one hour. After confirming by the gas chromatograph of the reaction mixture that the glycidyl ether completely disappeared, the reaction mixture was poured into a dilute aqueous solution of sodium bicarbonate whereby the acid was neutralized. Ether was added thereto and the mixture was stirred, and thereafter the ether layer was collected by separation. Anhydrous sodium sulfate was added for dehydration, and the solvent was removed by distillation under a reduced pressure thereby to obtain 68.8 g (yield: 90%) of colourless, transparent 2,2-dimethyl-4-oleyloxymethyl- 1,3-dioxolan.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04465869
Source datasetuspto-grants-1984_08
ORD IDord-70008f4373ea41da99ddb88554680db1
Source noteuspto-grants-1984_08