HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 18510272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromomethylstyrene | HCID 98116 | — |
| Reactant | HCID 18510222 | HCID 18510222 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18510272 | HCID 18510272 | — |
Reaction Steps
To 1-(5-bromo-3-pyridinyl)-2-[4-(methylsulfanyl)phenyl]-1-ethanone in DMF (2.5 mL) at 0° C. was added NaH (15 mg, 0.5 mmole). The reaction was stirred 30 minutes, at which point cinnamyl bromide (0.1 g, 0.5 mmole) was added and the reaction was allowed to warm to room temperature. The reaction was quenched with H2O and extracted with ethyl acetate. The organic phase was 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-6af79293ac3740d7b1e501e0d56e5bce |
| Source note | uspto-grants-2003_06 |