HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032337Generated: November 1, 2026
Potassium Iodide → 1-[3-(Diphenylmethoxy)propyl] 3-(3-methoxyphenyl)pyrrolidine
https://huagongshe.com/reaction/1032337
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(3-Methoxyphenyl)pyrrolidine | HCID 12937991 | — |
| Reactant | 1-(Diphenylmethoxy)-3-bromopropane | HCID 14306367 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[3-(Diphenylmethoxy)propyl] 3-(3-methoxyphenyl)pyrrolidine | HCID 14556309 | 51.3% |
Reaction Steps
A solution of 5.3 g (50 mmole) of 1-(diphenylmethoxy)-3-bromopropane in 50 cm3 of dimethylformamide was added to a mixture of 8.8 g (50 mmole) of 3-(3-methoxyphenyl)pyrrolidine, 13.8 g (100 mmole) of potassium carbonate, a few potassium iodide crystals and 250 cm3 of dimethylformamide. The reactive medium was heated to 80° C. for 12 hours and then filtered after it returned to room temperature. The filtrate was concentrated to dryness under reduced pressure. The residue was taken up with ether and extracted with 500 cm3 of N hydrochloric acid. The aqueous phase was separated, basified with 10N sodium hydroxide solution and extracted with methylene chloride. The organic solution was dried on sodium sulfate. Evaporation of the solvent yielded an oily residue, which was purified by silica gel column filtration (eluent, hexane-ethyl acetate, 1/1). There was obtained 10.3 g (yield: 51.3%) of 1-[3-(diphenylmethoxy)propyl] 3-(3-methoxyphenyl)pyrrolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04957927 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-ffb1ceabd32a4e57b42e4156244a95cc |
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| Source note | uspto-grants-1990_09 |
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