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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943270Generated: October 26, 2026

Pyrrolidine → 1-(3,5-Difluorobenzyl)pyrrolidine

https://huagongshe.com/reaction/1943270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantSodium BicarbonateHCID 516892—
Reactant3,5-DifluorobenzaldehydeHCID 588160—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(3,5-Difluorobenzyl)pyrrolidineHCID 6727925274%

Reaction Steps

3,5-Difluorobenzaldehyde (2.0 mL, 18.24 mmol), pyrrolidine (1.8 mL, 21.56 mmol), and sodium triacetoxyborohydride (5.8 g, 27.4 mmol) were stirred in THF (50 mL) for 16 h at room temperature. Saturated aqueous NaHCO3 (30 mL) was added and after stirring for 30 min, EtOAc (50 mL) was added. The organic phase was separated and washed with brine, dried over MgSO4 and concentrated to afford 2.65 g (74%) of 1-(3,5-difluorobenzyl)pyrrolidine as a slightly cloudy oil: 1H NMR (CDCl3) δ 6.88-6.83 (m, 1H), 6.68-6.63 (m, 2H), 3.59 (s, 2H), 2.53-2.48 (m, 4H), 1.80-1.77 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389743B2
Source datasetuspto-grants-2013_03
ORD IDord-25505d1f39fb4b058ff584721ce1637e
Source noteuspto-grants-2013_03