Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Dodecanol | HCID 8193 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Product | Dilauryl Ether | HCID 20667 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07375095B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-a5ec998d1d904bc99488f6ceaa5eceb1 |
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| Source note | uspto-grants-2008_05 |
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