HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → N-(3,4-Dichlorophenyl)-2-[3-(phenylmethoxy)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(3,4-dichlorophenyl)-2-(3-hydroxyphenyl)acetamide | HCID 23440791 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(3,4-Dichlorophenyl)-2-[3-(phenylmethoxy)phenyl]acetamide | HCID 23440880 | 64% |
Reaction Steps
To a solution of N-(3,4-dichlorophenyl)-2-(3-hydroxyphenyl)acetamide (5.5 g, 0.019 mol) in DMF (25 ml) was added potassium carbonate powder (3.93 g, 0.028 mol). To the flask was added benzyl bromide (2.37 ml, 0.021 mol). The reaction was allowed to stir overnight. Solvent was removed and the reaction was diluted with ethyl acetate. The organic layer was washed with water, dried over MgSO4, filtered and concentrated. The crude product was triturated with ether and hexanes to provide the title compound (4.65 g, 64% yield): ES-MS (m/z) 386 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435729B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-ef0eb6f308fe4ace8078341cf7e80b3e |
| Source note | uspto-grants-2008_10 |