Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Propylene Carbonate | HCID 7924 | — |
| Reactant | Propylene | HCID 8252 | — |
| Solvent | Water | HCID 962 | — |
| Product | Propanal | HCID 527 | — |
| Product | Propylene Glycol | HCID 1030 | — |
| Product | Propylene Oxide | HCID 6378 | — |
Reaction Steps
Into a 500 ml Hastelloy stirred autoclave, there was introduced 10.6 g of cuprous iodide, 9.24 g of potassium iodide, 6.15 g of cupric carbonate dihydroxide, 150 ml of water, 16.0 g of propylene, 600 psia of carbon dioxide, and 200 psia of oxygen. The reaction mixture was heated at 120° C. for 5 hours. The workup procedure was essentially the same as described in Example 1. The reaction produced 41 mmoles of propylene carbonate, 7 mmoles of propylene glycol, 7 mmoles of propylene iodohydrins, 7 mmoles of acetone, 2 mmoles of propanal, and 1 mmole of propylene oxide. The productivity rate amounted to 0.086 mole/liter-hour. In a comparison of Example 11 with Example 13, the use of ferrous iodide gave a higher productivity rate than that obtained using cuprous iodide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04247465 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-2ab11ecfcc26455f8fe02bc2655af73b |
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| Source note | uspto-grants-1981_01 |
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