HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248404Generated: October 25, 2026
Potassium Iodide → 3-{1-[4,4-bis-(4-Fluorophenyl)-1-butyl]-4-piperidinyl}-1,2-benzisothiazole hydrochloride
https://huagongshe.com/reaction/1248404
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,1'-(4-Chlorobutylidene)bis(4-fluorobenzene) | HCID 76820 | — |
| Reactant | 4-(3-Benzisothiazolyl) piperidine | HCID 13324093 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-{1-[4,4-bis-(4-Fluorophenyl)-1-butyl]-4-piperidinyl}-1,2-benzisothiazole hydrochloride | HCID 20255753 | 21% |
Reaction Steps
A mixture of 5.0 g of 3-(4-piperidinyl)-1,2-benzisothiazole, 7.70 g of 4-chloro-1,1-bis(4-fluorophenyl)butane, 7.0 g of potassium carbonate, 0.25 g of potassium iodide and 120 ml of dimethylformamide was stirred at 90° for 8.0 hrs and overnight at ambient temperature. The reaction mixture was poured into water, extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The product was purified by high-pressure liquid chromatography using dichloromethane:methanol (2%) as the eluent. The eluent was evaporated, the residue was dissolved in ether and a saturated hydrogen chloride/ether solution was added dropwise to yield a solid. The solid was recrystallized from ethyl acetate/ether to give 2.0 g (21%) of product, mp 198°-199°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04524074 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-b39b42f96a684cba825d9dc67b616f5a |
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| Source note | uspto-grants-1985_06 |
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