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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419853Generated: October 26, 2026

Pyrrolidine → 1-(5-Chloro-2-nitrobenzyl)pyrrolidine

https://huagongshe.com/reaction/419853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant5-Chloro-2-nitrobenzaldehydeHCID 81123—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
Product1-(5-Chloro-2-nitrobenzyl)pyrrolidineHCID 783395—

Reaction Steps

Pyrrolidine (4 mL, 48.5 mmol) was added to a solution of 5-chloro-2-nitrobenzaldehyde (6 g, 32.2 mmol) in dichloromethane (150 mL) and the solution was stirred at room temperature for 30 minutes. The solution was then cooled in ice, and sodium triacetoxyborohydride (10.3 g, 48.5 mmol) was added portionwise. Once addition was complete, the reaction was stirred at room temperature for 4 hours. The reaction was washed with sodium carbonate solution, dried over MgSO4 and evaporated under reduced pressure. The residual oil was purified by column chromatography on silica gel using ethyl acetate:pentane (86:14) to afford the title compound as a pale yellow solid, 6.3 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093400B2
Source datasetuspto-grants-2012_01
ORD IDord-4d36990dc3cd4d02b52bfdff2406ea4c
Source noteuspto-grants-2012_01