HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466618Generated: October 31, 2026
Potassium Iodide → HCID 19814359, compound
https://huagongshe.com/reaction/466618
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 11187396 | HCID 11187396 | — |
| Reactant | HCID 19814230 | HCID 19814230 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | HCID 19814359 | HCID 19814359 | 79.3% |
Reaction Steps
A mixture containing 7.27 g of 3-butyl-4-hydroxy-4-methyl-2-oxo-1-oxa-3,8-diazaspiro[4,5]decane, 12.89 g of 4,4-bis(4-chlorophenyl)-3-butenyl bromide, 4.98 g of anhydrous potassium carbonate and 0.6 g of potassium iodide in 73 ml of methyl isobutyl ketone is gently refluxed under argon while stirring for 6 hours. After cooling down, the inorganic salts are filtered off, washed with methyl isobutyl ketone, the filtrate is washed with water to neutral, dried over anhydrous magnesium sulfate and then the solvent is distilled off under reduced pressure. After recrystallizing the evaporation residue from ethanol, the product obtained is dissolved in ether and the hydrochloride is precipitated by adding ethereal hydrogen chloride solution to obtain 79.3% of the title hydrochloride, m.p.: 230°-233° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05157038 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-afb1622deac741dc89e02a0bd0575f0b |
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| Source note | uspto-grants-1992_10 |
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