Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycerol | HCID 753 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Catalyst | Palladium acetylacetonate | HCID 5486778 | — |
| Catalyst | Trisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate) | HCID 6099338 | — |
| Solvent | Water | HCID 962 | — |
| Product | Octadienyl glyceryl ether | HCID 54098056 | 72.9% |
Reaction Steps
In a 500-mL autoclave, charged were 70 g (0.76 mol) of glycerin, 0.7 g (2.3 mmol) of bis(acetylacetonato)palladium (II), 3.0 g (5.3 mmol) of triphenylphosphine-3,3′,3″-trisulfonic acid trisodium salt and 35 g of water. The mixture was heated to 80° C., whereby a water-soluble liquid phase was obtained. After cooling, 180 g (3.3 mol) of 1,3-butadiene was introduced at a time into the autoclave as a hydrocarbon solvent phase. While stirring, the mixture was heated to 80° C. again. The initial pressure in the autoclave showed 1.0 MPa. After stirring at 80° C. for 10 hours, the water phase and unreacted butadiene were removed, followed by washing with water, whereby 111 g of octadienyl glyceryl ether was obtained as a pale yellow transparent oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06504063B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-c7e8311bc0de4f0089ce0d9ec0e10097 |
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| Source note | uspto-grants-2003_01 |
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