HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2-Chloro-6-(l-iodomethylvinyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Chloro-6-(3-chloroprop-1-en-2-yl)pyridine | HCID 15008711 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-6-(l-iodomethylvinyl)pyridine | HCID 15008714 | 60.6% |
Reaction Steps
A mixture of 0.50 g of 2-chloro-6-(1-chloromethylvinyl) pyridine, 0.88 g of potassium iodide, 5 ml of acetone and 0.5 ml of N,N-dimethylformamide was stirred at 50° to 60° C. for 5 hours. After the reaction mixture was cooled to room temperature, water was added thereto to extract the mixture with ethyl acetate. The extract was subsequently washed with an aqueous solution of 10% sodium thiosulfate, water, saturated saline solution in that order, and dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (eluted with dichloromethane) to obtain 0.45 g of the objective compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960897 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-f359e0db42334c3cb960a771f72f3bea |
| Source note | uspto-grants-1990_10 |