HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931810Generated: October 26, 2026
Iodoethane → 3-(3-Chloro-2-fluorophenyl)-1-ethylpyrrolidin-3-ol
https://huagongshe.com/reaction/1931810
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(3-Chloro-2-fluorophenyl)pyrrolidin-3-ol | HCID 68515744 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(3-Chloro-2-fluorophenyl)-1-ethylpyrrolidin-3-ol | HCID 25143670 | — |
Reaction Steps
In a sealed tube a mixture of 3-(3-chloro-2-fluorophenyl)pyrrolidin-3-ol (0.5 g, 2.32 mmol), acetonitrile (3 mL), potassium carbonate (0.48 g, 3.48 mmol) and iodoethane (0.36 g, 2.32 mmol) was heated under microwave irradiation at 120° C. for 20 minutes. Aqueous sodium carbonate (10%, 50 mL) was added and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic phase was dried (Na2SO4) and evaporated. Purification by HPLC on Waters OBD C18, 5 μm (MeOH/33 mM NH3, 20:80 to 50:50) gave the title compound. The amine was converted to the fumaric acid salt and recrystallized from methanol/diethyl ether/diisopropyl ether (0.249 g). M.p. 142-145.5° C.; MS m/z (relative intensity, 70 eV) 243 (M+, 24), 228 (19), 157 (15), 72 (27), 71 (bp).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188301B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-28bc2775f5854e0bbe554760e6ed6712 |
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| Source note | uspto-grants-2012_05 |
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