HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 5-Chloro-2-[2-(6-chloro-2-pyridyl)propen-3-yl]-2-methylindan 1,3-dion
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Chloro-6-(3-chloroprop-1-en-2-yl)pyridine | HCID 15008711 | — |
| Reactant | 5-Chloro-2-methylindan-1,3-dione | HCID 53930449 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Chloro-2-[2-(6-chloro-2-pyridyl)propen-3-yl]-2-methylindan 1,3-dion | HCID 15116818 | 87% |
Reaction Steps
In 20 ml of methanol was dissolved 1.32 g of 85% potassium hydroxide, and then 3.89 g of 5-chloro-2-methylindan-1,3-dione, 3.76 g of 6-chloro-2-(1-chloromethylvinyl)pyridine and 0.05 g of potassium iodide were added to the solution. After refluxing under heating for 3 hours, the solvent was evaporated and water was poured. The reaction mixture was extracted with ethyl acetate, the organic layer was washed with water and with a saturated saline solution, and then dried over anhydrous magnesium sulfate. After the solvent was evaporated, the residue was separated and purified by silica gel column chromatography (developing solvent: n-hexane/ethyl acetate=5/1) to obtain 6.02 g of the compound No. 115 shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05076830 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-ede28d899e7843c5873d4f5d0c3499ea |
| Source note | uspto-grants-1991_12 |