HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-(2,5-Difluorophenyl)pyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(2,5-difluorophenyl)-3,4-dihydro-2H-pyrrole | HCID 58335726 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2,5-Difluorophenyl)pyrrolidine | HCID 24697858 | — |
Reaction Steps
In step 6A-3, sodium borohydride (2.1 g, 55.2 mmol) was added at room temperature to a solution of 5-(2,5-difluorophenyl)-3,4-dihydro-2H-pyrrole (6-4) (5.0 g, 28 mmol) in anhydrous ethanol (150 mL). The reaction mixture was stirred over-night at room temperature. The ethanol was removed using a rotary evaporator and the resulting orange solid was reconstituted with ethyl acetate. The organic layer was washed with brine (3×150 mL), dried with sodium sulfate and the. ethyl acetate was removed to yield 2-(2,5-difluorophenyl)pyrrolidine (6-5) as a light yellow oil. m/z=184.2 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507488B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-d911cd8a478e43d4ae312e818155d80c |
| Source note | uspto-grants-2013_08 |