HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylhydroquinone → tert-Butyl-1,4-benzoquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylhydroquinone | HCID 16043 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-Butyl-1,4-benzoquinone | HCID 19211 | — |
Reaction Steps
30 g. of tert-butylhydroquinone (Eastman-Kodak) were dissolved in 200 ml. of anhydrous ether and 30 g. of anhydrous sodium sulfate were added. To this mixture was added 60 g. of silver oxide in small increments. An exothermic reaction ensued. After shaking for 20 minutes, the reaction mixture was filtered and the filtrate evaporated under the hood. Yellow crystals of tert-butyl-p-benzoquinone were obtained melting at 55°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04058568 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-d49d48db05ea4227a633fbbe89941bac |
| Source note | uspto-grants-1977_11 |