HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylprop-2-En-1-Ol → 2-Propenoic acid, 3-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylprop-2-En-1-Ol | HCID 308 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Propenoic acid, 3-phenyl- | HCID 8784 | 96.3% |
Reaction Steps
In an ambient pressure oxygen atmosphere, 40.3 mg of cinnamyl alcohol, 105.3 mg of the platinum catalyst obtained in Example 1 and 40.2 mg of potassium carbonate were agitated for eighteen hours at 60° C. in 3 ml of water. The aqueous layer was subsequently washed using tert-butyl methyl ether and was extracted using ethyl acetate after neutralizing the layer with a HCl solution. The ethyl acetate solution was dried using magnesium sulfate, filtered and concentrated to obtain 41.5 mg (93% yield) of cinnamic acid. The reaction equation and the analytical results of the product are shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897817B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-8181723e5da3472a9ecdbf0f0398a5a4 |
| Source note | uspto-grants-2011_03 |