HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 18510254, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromomethylstyrene | HCID 98116 | — |
| Reactant | HCID 18510213 | HCID 18510213 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18510254 | HCID 18510254 | — |
Reaction Steps
To a solution of 2-[4-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]-1-phenyl 1-ethanone (0.2 g, 0.72 mmole) in DMF (3 mL) was added NaH (0.022 g, 0.7 mmole) at 0° C. The reaction was stirred for 15 min. Then a solution of cinnamyl bromide (0.16 g, 0.84 mmol) in 1 mL DMF was added. The reaction was warmed to room temperature, and was then quenched with saturated NH4Cl solution and extracted with ethyl acetate. The organic phase was then dried (Na2SO4), filtered, and evaporated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06583126B2 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-3197a6f1842340548a93e02dbc9f31c8 |
| Source note | uspto-grants-2003_06 |