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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890682Generated: October 30, 2026

Sodium borohydride → 2-(2,5-Difluorophenyl)pyrrolidine

https://huagongshe.com/reaction/1890682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(2,5-difluorophenyl)-3,4-dihydro-2H-pyrroleHCID 58335726—
SolventEthanolHCID 702—
Product2-(2,5-Difluorophenyl)pyrrolidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507488B2
Source datasetuspto-grants-2013_08
ORD IDord-d911cd8a478e43d4ae312e818155d80c
Source noteuspto-grants-2013_08