HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluoronitrobenzene → 2,6-Ditert-butyl-4-(4-nitrophenyl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2,6-Ditert-butyl-4-(4-nitrophenyl)phenol | HCID 1734905 | — |
Reaction Steps
8.40 g (40.7 mmol) 2,6-di-tert-butylphenol was dissolved in 100 ml dried DMSO. 8 g (58 mmol) potassium carbonate and 7.6 g (54 mmol) p-fluoronitrobenzene were added into the DMSO solution. The DMSO solution was heated to 100˜120° C. for 12 hrs with stirring. Then the reaction mixture was allowed to cool to room temperature and poured into distilled water. The aqueous solution was acidified to pH 2˜4 and yellow precipitate was collected by filtration. The yellow precipitate was washed with water and dried. The crude yield was 75%. The yellow precipitate was purified by recrystallizing in cyanomethane, mp 157˜160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07317110B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-63242472b8d54ccd9230861bfa7c5199 |
| Source note | uspto-grants-2008_01 |