HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2,6-Di-tert-butyl-4-hydroxy-4-methyl-2,5-cyclohexadienone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | Bistrifluoroacetoxyiodobenzene | HCID 12041285 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | 2,6-Di-tert-butyl-4-hydroxy-4-methyl-2,5-cyclohexadienone | HCID 146102 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 5.0 g of 2,6-di-t-butyl-p-cresol in 90 ml of acetonitrile/water (5/1) was added 10.5 g of bistrifluoroacetoxyiodobenzene with stirring at 0° C. After stirring for 30 minutes, 90 ml of water was added and the reaction solution was extracted three times with 50 ml of dichloromethane and washed four times with 60 ml of water. Organic layers were dried over anhydrous sodium sulfate, then concentrated under reduced pressure and the precipitating crystal was filtered to give a crude crystal, which was recrystallized from hexane to give 4-methyl-4-hydroxy-2,6-di-t-butylcyclohexa-2,5-diene-1-one as a pale yellow solid. The yield was 3.0 g (55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06280893B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-ec6e649ed0ab460da14e321f0da99a51 |
| Source note | uspto-grants-2001_08 |