HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 14229165, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (3-bromoprop-1-en-2-yl)benzene | HCID 234998 | — |
| Reactant | 4-Cyano-N-methylbenzenesulfonamide | HCID 15672484 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14229165 | HCID 14229165 | 46.4% |
Reaction Steps
To a mixture of 2.30 g of 4-cyano-N-methylbenzenesulfonamide, 2.40 g of α-(bromomethyl)styrene and 20 ml of N,N-dimethylformamide, 0.63 g of 50% sodium hydride (oil dispersed) was slowly added with stirring under ice cooling, then the mixture was stirred at room temperature for 6 hours. After evaporating the solvent under a reduced pressure, ethyl acetate was added to the residue. The organic layer was washed with water and dried over anhydrous sodium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (developing solvent: ethyl acetate n-hexane) to obtain 1.70 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04971620 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-4cf675f2292f473e8bef82312a2907b1 |
| Source note | uspto-grants-1990_11 |