HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745319Generated: October 31, 2026
Potassium Iodide → HCID 13319852, compound
https://huagongshe.com/reaction/745319
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4-Phenylpiperidine | HCID 69873 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazole | HCID 10910880 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13319852 | HCID 13319852 | 53.8% |
Reaction Steps
To 30 ml of dry dimethylformamide was added 2.4 g of 4-phenylpiperidine, 3.4 g of 3-(3-chloropropyl)-6-fluoro-1,2-benzisoxazole, 8.0 g of sodium bicarbonate, and a few crystals of potassium iodide. After stirring at 100° C. for three hrs, the mixture was filtered and the filtrate was evaporated to an oil. The oil was stirred with 100 of ml water for five mins and then extracted into ether. The ether extract was washed with water (2×), saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, the solvent was evaporated to an oil. The oil was dissolved in ether and treated with ethereal hydrogen chloride, and the resultant salt was twice recrystallized from ethyl acetate/methanol/ether to give 3.0 g (53%) of product, mp 213°-214° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04598152 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-13804d90665c4644b0548e1c2de21427 |
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| Source note | uspto-grants-1986_07 |
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