HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904294Generated: October 30, 2026
Potassium Iodide → HCID 23334048, compound
https://huagongshe.com/reaction/904294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22226923 | HCID 22226923 | — |
| Reactant | 4-Hydroxy-3-methyl-2H-chromen-2-one | HCID 54687016 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | HCID 23334048 | HCID 23334048 | 67% |
Reaction Steps
8.8 g. (0.05 mol) of 3-methyl-4-hydroxy-coumarin are solubilised in 200 ml. of methyl isobutyl ketone at 80° C., and then, at this temperature, there are added 8.3 g. (0.06 mol) of anhydrous potassium carbonate and 0.5 g. of potassium iodide. The mixture is left for 1 hour at 80° C. while stirring. In 1 hour, there is added a solution of 9.8 g. (0.065 mol) of 2-morpholino-2-chlorethane in 50 ml. of methyl isobutyl ketone. The substance is then refluxed for 8 hours, filtered while hot and evaporated under vacuum. The oil which is obtained is taken up under heat in 200 ml. of a 5% solution of sodium bicarbonate, whereafter it is cooled, and extracted with 3×100 ml of ether. It is dried over NaSO4 and then the ether is evaporated under vacuum. A brown oil is obtained which cannot be crystallised. Weight 10 g.; yield 67% (theoretical yield 14.9 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04230850 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-ce041516a6aa481b9c667b53bb34e733 |
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| Source note | uspto-grants-1980_10 |
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