HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-(benzyloxy)-N-phenylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Hydroxydiphenylamine | HCID 31208 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(benzyloxy)-N-phenylaniline | HCID 296079 | — |
Reaction Steps
To a solution of 4-hydroxy-N-phenyl-aniline (30 g; 162 mmol) in acetonitrile (400 mL) there are added 58 g of Cs2CO3 (178 mmol) and stirring is carried out for 15 minutes at ambient temperature. Benzyl bromide (22.5 mL; 178 mmol) is then added dropwise and then the reaction mixture is refluxed for 4 hours. After filtering and rinsing with acetonitrile, the filtrate is concentrated and purified by chromatography over silica gel using petroleum ether and ethyl acetate as eluants. The title product is then obtained in the form of a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108983B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-e33c16b7ac2b48169432ff3da3fed603 |
| Source note | uspto-grants-2015_08 |