HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-Benzyloxy-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Amino-3-Nitrophenol | HCID 3758882 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 4-Benzyloxy-2-nitroaniline | HCID 261497 | — |
Reaction Steps
28.87 g (187.5 mM) of 2-nitro-4-hydroxyaniline in 600 ml of methyl ethyl ketone (MEK) are treated with 77.6 g of potassium carbonate and 22.3 ml (187.5 mM) of benzyl bromide. The reaction mixture is heated at reflux for3 h and is then evaporated to dryness. The evaporation residue is triturated in hexane, is filtered and dried under vacuum. There are thus isolated 40 g (88.9%) of the expected derivative, of melting point 106° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446059 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-bdb4fd7dae9340d8b9add6230c52541b |
| Source note | uspto-grants-1995_08 |