HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Benzyloxy-3-ethyl-5-methylphenyl benzoate → 2-Ethyl-6-methyl-4-benzoyloxyphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Benzyloxy-3-ethyl-5-methylphenyl benzoate | HCID 54236096 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Ethyl-6-methyl-4-benzoyloxyphenol | HCID 23282409 | 95% |
Reaction Steps
Then, 8.4 g of crude 4-benzyloxy-3-ethyl-5-methylphenyl benzoate was 5 dissolved in 100 ml of ethyl acetate, which was put into a reaction vessel, and the air in the vessel was replaced with nitrogen gas. Then, 0.5 g of 10% palladium on carbon was added, and the nitrogen gas in the vessel was replaced with hydrogen gas, followed by vigorous stirring at room temperature for 24 hours. The hydrogen gas in the vessel was replaced with nitrogen gas, after which the reaction mixture was filtered through cerite and the filtrate was concentrated under reduced pressure, which afforded 5.9 g of crude 3-ethyl-4-hydroxy-5-methylphenyl benzoate (95% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214835B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-45eeaeb8b8a34e5391c59ef01064f624 |
| Source note | uspto-grants-2001_04 |