HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224611Generated: October 26, 2026
Potassium Iodide → 1'-[3-(4-Fluorobenzoyl)propyl]-1-methyl-2-oxo-indoline-3-spiro-4'-piperidine
https://huagongshe.com/reaction/224611
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(3-Chloropropyl)-2-(4-fluorophenyl)-1,3-dioxolane | HCID 2723778 | — |
| Reactant | 1-Methylspiro[indoline-3,4'-piperidin]-2-one | HCID 21584155 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1'-[3-(4-Fluorobenzoyl)propyl]-1-methyl-2-oxo-indoline-3-spiro-4'-piperidine | HCID 70592316 | — |
Reaction Steps
A mixture of 3.0 g of 4-chloro-1-(4-fluorophenyl)-1,1-ethylenedioxybutane, 2.0 g of 1-methyl-2-oxo-indoline-3-spiro-4'-piperidine, 2.8 g of anhydrous potassium carbonate, 0.1 g of potassium iodide and 30 ml of dimethylformamide was refluxed for 2 hours. The resulting mixture was poured into water and was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and concentrated in vacuo. To the residual oil were added 60 ml of methanol, 20 ml of water and 10 ml of concentrated hydrochloric acid. The mixture was refluxed for 25 minutes and concentrated in vacuo. The residual oil was made alkaline with 28% aqueous ammonia and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and concentrated. The residual oil was chromatographed over silica gel with ethyl acetate as an elueting agent to give 1'-[3-(4-fluorobenzoyl)propyl]-1-methyl-2-oxo-indoline-3-spiro-4'-piperidine, M.P. 95°-96.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04233307 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-9ae4a1c19e7b4a739b433df2aacfd6d7 |
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| Source note | uspto-grants-1980_11 |
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