HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → Trimethylhydroquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 2,3,5-Trimethylphenol | HCID 12769 | — |
| Reactant | Indium sulfate | HCID 26044 | — |
| Reactant | 3,4,6-Trimethylbenzene-1,2-diol | HCID 12551190 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | Trimethylhydroquinone | HCID 12785 | — |
Reaction Steps
In a vessel used in Example 52 were placed 100 g. (735 m. moles) of 2,3,5-trimethylphenol, 2.31 g. (23.1 m. moles) of 4-methyl-2-pentanone, 2.61 g. (46.0 m. moles) of 60 percent hydrogen peroxide and 1.0 g. of indium sulphate (In2 (SO4)3.9H2O), and the mixture was treated at 100° C. for 60 minutes. 2.16 g. (14.2 m. moles) of 3,4,6-trimethylcatechol and 0.64 g. (4.2 m. moles) of 2,3,5-trimethylhydroquinone were obtained. The yield of dihydric alkylphenols was 40.0 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04078006 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-69e61c38a18f416c8986130751808002 |
| Source note | uspto-grants-1978_03 |