HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Hydroxy-4,6-dimethylphenyl)-1-butanone → 2-Butyl-3,5-dimethylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Hydroxy-4,6-dimethylphenyl)-1-butanone | HCID 4201006 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Perchloric Acid | HCID 24247 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Butyl-3,5-dimethylphenol | HCID 20209997 | — |
Reaction Steps
10 g. of 2-butyryl-3,5-dimethyl-phenol are dissolved in 100 ml. of glacial acetic acid. After the addition of 3 drops of perchloric acid, the solution is hydrogenated under normal conditions in the presence of 0.5 g. of platinum oxide. After the uptake of 3.0 l. of hydrogen, the hydrogenation is stopped. The catalyst is filtered off. The filtrate is extracted with ether. The ether extract is washed with water to neutral reaction, dried over sodium sulfate and evaporated. There is obtained 2-butyl-3,5-dimethylphenol, which melts at 65°-67° C. after absorption on silica gel, using methylene chloride/hexane 1:1 parts by volume as the eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04319048 |
| Source dataset | uspto-grants-1982_03 |
| ORD ID | ord-8795ef2d8def4a568fe09faf2331d61c |
| Source note | uspto-grants-1982_03 |