HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2,4-Dichlorophenyl)-1-(3-pyridyl)-1-propanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Dichlorobenzyl 3-pyridyl ketone | HCID 13671239 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2,4-Dichlorophenyl)-1-(3-pyridyl)-1-propanone | HCID 14074431 | — |
Reaction Steps
28 g of 2,4-dichlorobenzyl 3-pyridyl ketone are dissolved in 800 ml of dimethylformamide and treated portionwise at 0° C. with 5.5 g of sodium hydride (50% dispersion in oil). After 2 hours at room temperature 14.9 g of methyl iodide are added and the mixture is stirred at room temperature for a further 3 hours. The mixture is then poured into water and extracted with diethyl ether. The organic phase is washed, dried over anhydrous sodium sulfate and subsequently concentrated. By chromatography on silica gel with n-hexane/ethyl acetate (1:2) there is obtained 2-(2,4-dichlorophenyl)-1-(3-pyridyl)-1-propanone as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04753947 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-0a4b726cdd534cdf9af701c71168eea2 |
| Source note | uspto-grants-1988_06 |