HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 3-benzyloxy-2-nitro-N-methylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-fluoro-N-methyl-2-nitroaniline | HCID 54489739 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-benzyloxy-2-nitro-N-methylaniline | HCID 10729890 | 100% |
Reaction Steps
Benzyl alcohol (9.54 mL, 92.2 mmol), tetrabutyl ammonium bromide (1.49 g, 4.62 mmol), and potassium carbonate (7.64 g, 55.3 mmol) were added to a toluene solution (39 mL) of 3-fluoro-N-methyl-2-nitroaniline (7.84 g, 46.1 mmol), and the mixture was heated under reflux for 6 hours. The reaction solution was cooled, and water (39 mL) was added thereto, followed by toluene extraction. The resulting organic layer was washed with water, and the solvent was distilled off under reduced pressure, thereby obtaining 11.9 g of a red, powdery target compound (yield: 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08940889B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-36111e3a7df94f0c88679ea55cd1d94a |
| Source note | uspto-grants-2015_01 |