HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233028Generated: October 25, 2026
Iodoethane → 3-[1-Ethyl-2-pyrrolidinyl]phenol
https://huagongshe.com/reaction/233028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(3-Methoxyphenyl)pyrrolidine | HCID 3613824 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-[1-Ethyl-2-pyrrolidinyl]phenol | HCID 23361312 | 26% |
Reaction Steps
To a solution of 2-(3-methoxyphenyl)pyrrolidine (3.5 g) in dry acetonitrile (60 ml) was added milled potassium carbonate (4.1 g), followed by iodoethane (1.3 ml) at ambient temperature, under nitrogen, with stirring for 7 hrs. The reaction mixture was filtered through a pad of celite and the filter cake was washed with ethyl acetate. The combined filtrates were concentrated and the residue was diluted with 48% hydrobromic acid (30 ml) and warmed at 100° C. for 3.5 hrs. Upon cooling to ambient temperature, the reaction mixture was neutralized with saturated sodium bicarbonate solution and the filtrate was extracted with dichloromethane (2 times). The combined organics were dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, dichloromethane/0-10% methanol). The appropriate fractions were collected and concentrated to give 0.8 g (26%) of 3-[1-ethyl-2-pyrrolidinyl]phenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591856 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-16e59a0ff9084c18a80d4092a426c0b3 |
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| Source note | uspto-grants-1997_01 |
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