HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-(Benzyloxy)-2-chloro-1-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3-Chloro-4-nitrophenol | HCID 10283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(Benzyloxy)-2-chloro-1-nitrobenzene | HCID 819861 | — |
Reaction Steps
A mixture of 3-chloro-4-nitrophenol (10 g, 0.058 mole), benzyl bromide (11.8 g, 0.069 mole), and potassium carbonate (16 g, 0.116 mole) in acetone is stirred, heated at reflux temperature for 17 hours, cooled and filtered. The filtrate is concentrated in vacuo to give a solid residue which is recrystallized from absolute ethanol to give the title compound, mp 82°-84.5° C., identified by elemental and NMR analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05686617 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-6c58a18e95044d748314a8edd22ea2ba |
| Source note | uspto-grants-1997_11 |