HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-(3-fluorophenyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(3-fluorophenyl)-3,4-dihydro-2H-pyrrole | HCID 12009049 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3-fluorophenyl)pyrrolidine | HCID 3912402 | 69.2% |
Reaction Steps
To a stirred solution of 5-(3-fluoro-phenyl)-3,4-dihydro-2H-pyrrole (1.10 g, 6.74 mmol) in methanol (40 ml) was added at 0° C. sodium borohydride (0.51 g, 13.4 mmol) and the reaction mixture was stirred at RT for 1 h. Then additional sodium borohydride (0.25 g, 6.61 mmol) was added and stirring was continued for 1 h. The mixture was evaporated, dissolved in saturated NaHCO3-solution (70 ml) and extracted with dichloromethane (2×70 ml). The combined organic layers were washed with brine (70 ml), dried (MgSO4) and evaporated. The crude product was purified by column chromatography on silica gel (dichloromethane/MeOH/NH4OH 15:1:0.1) to give the product (0.77 g, 69%) as a colorless oil, MS: m/e=165 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06284785B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-433d9dd8e2504b82994092988a61f437 |
| Source note | uspto-grants-2001_09 |