HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478683Generated: October 29, 2026
Potassium Iodide → HCID 10665070, compound
https://huagongshe.com/reaction/478683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Butyne, 3-chloro-3-methyl- | HCID 70679 | — |
| Reactant | HCID 10540475 | HCID 10540475 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10665070 | HCID 10665070 | 44.4% |
Reaction Steps
To a solution of 2 g of the product of Step A in 50 ml of anhydrous dimethylformamide, under an inert atmosphere, there are added 2 g of anhydrous potassium carbonate. After stirring for 15 minutes at 65° C., 2.4 g of anhydrous potassium iodide and 4.4 g of 3-chloro-3-methyl-1-butyne are added, and the reaction mixture is held at 65° C. for 24 hours and then at 130° C. for 1 hour. After cooling, the solution is hydrolysed and then extracted with dichloromethane. The combined organic phases are washed with water and then with 1M potassium hydroxide solution, dried over sodium sulphate and then evaporated. After chromatography over silica gel (cyclohexane/acetone: 90/10), 1.10 g of the expected product are isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06642248B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-7b139e78e28c40b5a6266bd06556f2b7 |
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| Source note | uspto-grants-2003_11 |
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