HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (2-Ethylphenyl)acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-(2-Ethylphenyl)-1-propene | HCID 18694504 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Ethylphenyl)acetaldehyde | HCID 45117183 | — |
Reaction Steps
A solution of 54.05 g of the crude 1-allyl-2-ethylbenzene in 500 mL of 1:1 CH2Cl2 --CH3OH was cooled to -78° C. A stream of O3 was bubbled through the solution for 3 h, until all of the starting material had disappeared. Then a stream of air was bubbled through the solution until the blue color had faded. A total of 25 mL of methyl sulfide was added and the solution was stirred at room temperature for 1 h. The solution was concentrated and dried under vacuum to afford (2-ethylphenyl) acetaldehyde as a colorless oil which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06083980 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-b3450c4e848e46249f8835f1e8a263db |
| Source note | uspto-grants-2000_07 |