HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 68867323, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 68867329 | HCID 68867329 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68867323 | HCID 68867323 | — |
Reaction Steps
Benzyl bromide (0.02 mL, 0.179 mmol, d=1.438) and tetrabutyl ammonium iodide (catalytic amount) are added to a 0° C. suspension of 2-(2-Fluoro-phenoxy)-2-methyl-3-{4-[2-(3-methyl-2-oxo-imidazolidin-4-yl)-ethoxy]-phenyl}-propionic acid ethyl ester (0.053 g, 0.119 mmol) and sodium hydride (0.012 g, 0.298 mmol, 60% suspension on mineral oil), pre-stirred for 1 h at ambient temperature. The reaction mixture is stirred at ambient temperature for 18 h, diluted with ethyl acetate, and washed with 1N HCl, water, and brine. The organic layer is dried over MgSO4 and concentrated in vacuo to provide the title compound, which is carried into the next step. MS [EI+] 535 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07544812B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-b03bcbc6012547a7926b4fb38ef7fb25 |
| Source note | uspto-grants-2009_06 |