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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3-Chloropropyl)-2-(4-fluorophenyl)-1,3-dioxolaneHCID 2723778—
Reactant1-Methylspiro[indoline-3,4'-piperidin]-2-oneHCID 21584155—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1'-[3-(4-Fluorobenzoyl)propyl]-1-methyl-2-oxo-indoline-3-spiro-4'-piperidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04233307
Source datasetuspto-grants-1980_11
ORD IDord-9ae4a1c19e7b4a739b433df2aacfd6d7
Source noteuspto-grants-1980_11