HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3,5-Trimethylphenol → Trimethylhydroquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3,5-Trimethylphenol | HCID 12769 | — |
| Reactant | 3,4,6-Trimethylbenzene-1,2-diol | HCID 12551190 | — |
| Product | Trimethylhydroquinone | HCID 12785 | — |
Reaction Steps
By following in the same manner as in Example 56 except that 100 g. (735 m.moles) of 2,3,5-trimethylphenol was used instead of 3,5-dimethylphenol, 2.16 g. (14.2 m.moles) of 3,4,6-trimethylcatechol and 0.71 g. (4.7 m.moles) of 2,3,5-trimethylhydroquinone were obtained. The yield of dihydric alkylphenols was 44.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04072722 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-7f4c9c5a4c55467ca2bdd859f05d9ebf |
| Source note | uspto-grants-1978_02 |