HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Tert-Butylphenol → 1-tert-Butyl-2-(2-nitrophenoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Tert-Butylphenol | HCID 6923 | — |
| Reactant | 1-Chloro-2-nitrobenzene | HCID 6945 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-tert-Butyl-2-(2-nitrophenoxy)benzene | HCID 15415266 | 122.9% |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
A mixture of 2-chloronitrobenzene (9.5 g, 60 mmol), 2-t-butyl phenol (9.04 g, 60.2 mmol) and potassium carbonate (10.6 g) in DMF was heated at 130° C. for 6 days. The reaction was cooled to rt and partitioned between diethyl ether (400 mL) and water (500 mL). The organic layer was separated and the aqueous layer was extracted with ether (3×100 mL). The combined organic layers were dried over magnesium sulfate, filtered and evaporated to give 1-tert-butyl-2-(2-nitrophenoxy)benzene (20 g). (M+H)+=216.23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07470712B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-54406fba48aa4b17b8c686b64e9d12a1 |
| Source note | uspto-grants-2008_12 |