HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931814Generated: October 26, 2026
Iodoethane → 3-(3,4-Difluorophenyl)-1-ethylpyrrolidin-3-ol
https://huagongshe.com/reaction/1931814
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-(3,4-Difluorophenyl)pyrrolidin-3-ol | HCID 63586972 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(3,4-Difluorophenyl)-1-ethylpyrrolidin-3-ol | HCID 25143662 | 39.6% |
Reaction Steps
In a sealed tube a mixture of enantiomer E1 of 3-(3,4-difluorophenyl)pyrrolidin-3-ol (0.26 g, 1.3 mmol), acetonitrile (3 mL), potassium carbonate (0.269 g, 1.95 mmol) and iodoethane (0.20 g, 1.3 mmol) was heated under microwave irradiation at 80° C. for 25 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 washed with brine, dried (Na2SO4) and evaporated. Purification by HPLC on Waters OBD C18, 5 μm (MeOH/33 mM NH3, 35:65 to 50:50) gave the title compound (0.117 g). [α]D=+19.4° (methanol). The amine was converted to the fumaric acid salt and recrystallized from methanol/diethyl ether/diisopropyl ether: M.p. 136-137° C.; MS m/z (relative intensity, 70 eV) 227 (M+, 10), 207, (19), 141 (20), 72 (42), 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-5ec5579c2add408180d4fd5cb0c26ce0 |
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| Source note | uspto-grants-2012_05 |
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