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° 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 an additional 3 hours. Then the mixture is poured into water and extracted with diethyl ether, and the organic phase is washed and dried over anhydrous sodium sulfate and subsequently concentrated. The product is purified by chromatography on silica gel with n-hexane/ethyl acetate (1:2) to yield 2-(2,4-dichlorophenyl)-1-(3-pyridyl)-1-propanone as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04380544 |
| Source dataset | uspto-grants-1983_04 |
| ORD ID | ord-ada214616f2c4a279fe2d0c4100d5714 |
| Source note | uspto-grants-1983_04 |