Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Propylene | HCID 8252 | — |
| Product | Acetone | HCID 180 | 39% |
| Product | Propylene Oxide | HCID 6378 | 58% |
| Product | Propylene Carbonate | HCID 7924 | 4% |
Reaction Steps
Thallic oxide was again prepared as in Example 1. 4.0 g of thallic oxide (8.8 mmoles), 30 g water (1.7 moles), 80 g propylene (1.9 moles) and 95 g carbon dioxide (2.2 moles) were added to the autoclave in Example 1 which was then heated to 70° C. for 2.0 hours. The analysis showed 0.81 mmoles propylene oxide (58% yield), 0.55 mmoles acetone (39% yield) and 0.06 mmoles propylene carbonate (4% yield) to have formed. 1.40 mmoles of thallous bicarbonate (16% conversion) was detected in a solution having a pH =7.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04483996 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-03ceef9447a04ba2aed307993b77fa54 |
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| Source note | uspto-grants-1984_11 |
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