HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,3,6-Trimethylphenol | HCID 17016 | — |
| Product | 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl- | HCID 70291 | 28.6% |
Reaction Steps
13.6 g (0.1 mole) of 2,3,6-trimethylphenol was pulverized and dispersed in 40 g of water. Then, oxidation reaction was conducted in the same manner as in Example 4. The reaction proceeded so late that 2 hours were required at a room temperature. After conducting stream distillation, the same treatment as in Example 1 (B) was effected to obtain 4.28 g (28.6 percent in yield) of 2,3,6-trimethyl-p-benzoquinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03932475 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-7a677c81d11d42bdba4112a4e909d6de |
| Source note | uspto-grants-1976_01 |