Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,2-Epoxyoctadecane | HCID 23872 | — |
| Reactant | Magnesium orthosilicate | HCID 66225 | — |
| Solvent | Glycerol | HCID 753 | — |
| Product | Propylene Oxide | HCID 6378 | — |
| Product | 1,2-Epoxyoctadecane | HCID 23872 | — |
Reaction Steps
Thereafter, 1,2-epoxyoctadecane (385 parts) is added to the vessel with stirring and heating at 125° C. to 135° C. continued for another three hours or until at least 95% of the 1,2-epoxyoctadecane has reacted. The resulting product is treated with magnesium silicate (5% by weight) and water (1% by weight), heated at 120° C. for two hours, and filtered to remove residual potassium catalyst. Residual volatiles are removed by steam vacuum distillation (200°-205° C., 10 mm Hg vacuum, 3 parts water per part alkoxylated alcohol) to yield an alkoxylated alcohol containing an average of about 5 equivalents of reacted propylene oxide and 3 equivalents of reacted 1,2-epoxyoctadecane per equivalent of glycerin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05736174 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-4ea9a706c371418ea407947cb7ae2e51 |
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| Source note | uspto-grants-1998_04 |
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