HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 3-(3,4-Difluorophenyl)-1-ethylpyrrolidin-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| 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 | — |
Reaction Steps
Preparation according to Example 24: Enantiomer E2 of 3-(3,4-difluorophenyl)-pyrrolidin-3-ol (0.27 g, 1.35 mmol), acetonitrile (3 mL), potassium carbonate (0.279 g, 2.02 mmol) and iodoethane (0.21 g, 1.35 mmol). Purification by HPLC on Waters OBD C18, 5 μm (MeOH/33 mM NH3, 35:65 to 50:50). Yield 0.14 g. [α]D=−18.8° (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+, 11), 141, (20), 113 (17), 72 (43), 71 (bp).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188301B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-eb1db81b05334cca8e4351c8daa786ff |
| Source note | uspto-grants-2012_05 |