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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721995Generated: October 29, 2026

Ethylene Glycol → HCID 87904918, compound

https://huagongshe.com/reaction/721995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantSulfuric AcidHCID 1118—
Reactant1,2-EpoxydodecaneHCID 17858—
ReactantSodium BicarbonateHCID 516892—
ReactantCalcium ChlorideHCID 5284359—
SolventWaterHCID 962—
ProductHCID 87904918HCID 8790491899.5%

Reaction Conditions

Temperature62.5 °C

Reaction Steps

Separately, a 500 ml mixing vessel equipped with a calcium chloride-containing tube was charged with 276.5 g (1.50 moles) of 1,2-epoxydodecane. While the charged 1,2-epoxydodecane was stirred and cooled with water, a concentrated sulfuric acid was gradually dropped in an amount of 2.7 g (0.027 mole) into the cooled 1,2-epoxydodecane. After stirring for 15 minutes, the resultant mixture was placed into the dropping apparatus attached to the reaction vessel and was dropped into the ethylene glycol contained in the reaction vessel and maintained at a temperature of 60 to 65° C. over a time of 2 hours. Then the reaction of the mixture was carried out at a temperature of 60 to 65° C. for one hour. After the exhaustion of the starting material, namely 1,2-epoxydodecane, was confirmed by a thin-layer chromatography, the reaction was stopped. A powdered sodium hydrogen carbonate was mixed in an amount of 2.5 g (0.03 mole) into the resultant reaction liquid in the reaction vessel, the resultant mixture was stirred for 30 minutes to neutralize the reaction liquid. From the reaction liquid, precipitated crystals were separated by filtration. An 1,2-propanediol monohydroxydodecyl ether mixture was obtained in an amount of 395.4 g (yield: 99.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138365B2
Source datasetuspto-grants-2006_11
ORD IDord-41848e912451403d91ffbbc533778927
Source noteuspto-grants-2006_11