HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904305Generated: November 1, 2026
Potassium Iodide → HCID 23334095, compound
https://huagongshe.com/reaction/904305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4-(2-Chloroethyl)morpholine | HCID 76727 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 54702662 | HCID 54702662 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | HCID 23334095 | HCID 23334095 | 44.5% |
Reaction Steps
76.3 g. (0.3 mol) of 4,5-dihydroxy-3-phenyl-coumarin (Example 23a), 25.2 g. (0.3 mol) of sodium bicarbonate, 3 g. of potassium iodide and 800 ml. of methyl isobutyl ketone are brought over one hour to 80° C. The mixture is then cooled to 60° C., whereafter 48.4 g. (0.324 mol) of 2-morpholino-1-chlorethane are added dropwise and the temperature is brought over 8 hours to 100° C. It is then left at room temperature for one night and filtered. The precipitate obtained is taken up in 1 liter of chloroform. The light, insoluble substance obtained is filtered and the chloroform is evaporated under vacuum. The residue obtained is recrystallised from 700 ml. of methyl isobutyl ketone. 50 g. of a white product are isolated. M.P. 206° C.; yield 44.5% (theoretical yield 110.2 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-f69565ab3ccd4ea79b685c590f457d67 |
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| Source note | uspto-grants-1980_10 |
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