HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647304Generated: October 30, 2026
Potassium Iodide → HCID 13076453, compound
https://huagongshe.com/reaction/647304
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | (Chloromethyl)cyclopropane | HCID 80013 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(Piperidin-4-yl)benzo[d]isoxazole | HCID 13076436 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13076453 | HCID 13076453 | 48.4% |
Reaction Steps
To a suspension of 5.0 g of 3-(4-piperidyl)-1,2-benzisoxazole, 5.5 g of sodium bicarbonate and 3.0 g of potassium iodide in 75 ml of dimethylformamide was added, dropwise, 2.4 g of cyclopropylmethyl chloride in 25 ml of dimethylformamide, with stirring. The reaction was stirred at 80° for 20 hrs, cooled to room temperature and filtered. The filtrate was poured into 1 l of water and extracted with ether (three times). The ether extracts were washed with saturated sodium bicarbonate solution, saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was removed to give an oil, which was dissolved in ether into which sodium chloride was bubbled. The precipitate was collected and recrystallized twice from ethanol to give 3.5 g of product, mp, 234.5°-236°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04408053 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-288c0251aa73482db603706f1ed5217f |
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| Source note | uspto-grants-1983_10 |
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