Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223037Generated: November 1, 2026

1-Dodecanol → Dilauryl Ether

https://huagongshe.com/reaction/2223037

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-DodecanolHCID 8193—
ReactantSodium CarbonateHCID 10340—
Catalystp-Toluenesulfonic acidHCID 6101—
ProductDilauryl EtherHCID 20667—

Reaction Conditions

Temperature125 °C

Reaction Steps

After placing 390 parts by weight of n-dodecanol into a reaction vessel and heating to 125° C., one part by weight of p-toluene sulfonic acid as a catalyst was added to the solution, and then the pressure in the vessel was reduced to 5-10 mmHg. Separately, 100 parts by weight of anhydrous crystalline cyclotetrasaccharide, obtained by the method in Example B-3, was suspended in 130 parts by weight of n-dodecanol. The suspension was added into the above vessel drop by drop in a flow rate of 2.3 parts by weight/min with taking a time of 100 min for the reaction. Successively, the reactant was neutralized with aqueous sodium carbonate solution, and cyclotetrasaccharide dodecyl ether was obtained by evaporating residual alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375095B2
Source datasetuspto-grants-2008_05
ORD IDord-a5ec998d1d904bc99488f6ceaa5eceb1
Source noteuspto-grants-2008_05