HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259526Generated: October 30, 2026
Potassium Iodide → HCID 21412250, compound
https://huagongshe.com/reaction/259526
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | HCID 21412242 | HCID 21412242 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21412250 | HCID 21412250 | — |
Reaction Steps
A mixture of 30.7 g (0.1 mole) of 3,6-bis(2-chloroacetyl)acenaphthene, 100 ml of diethylamine and 2 g of potassium iodide is dissolved in 500 ml of tetrahydrofuran and allowed to stand in a stoppered flask for 8 days. The resulting amine salt which forms is filtered, washed with tetrahydrofuran and the combined filtrates reduced to dryness in vacuo. The residue is dissolved in methylene chloride, treated with charcoal and acidified using ethereal hydrochloric acid. The resulting solid which forms is filtered, recrystallized from a methanol-ether solution and further recrystallized from a methanol-ethyl acetate solution to yield a product, hygroscopic in nature, which indicated by its analysis to be a tetrahydrate having a m.p. 220.5°-222° C. (dec), λmax(EtOH) 283.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04038400 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-830ed16d132e428ab6113795c49e2da3 |
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| Source note | uspto-grants-1977_07 |
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