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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910452Generated: October 26, 2026

(3SR,4RS)-1-benzyl-3-(4-chloro-phenyl)-4-nitro-pyrrolidine → 1-Benzyl-4-(4-chlorophenyl)pyrrolidin-3-amine

https://huagongshe.com/reaction/910452

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3SR,4RS)-1-benzyl-3-(4-chloro-phenyl)-4-nitro-pyrrolidineHCID 66940656—
CatalystZincHCID 23994—
CatalystTitanium TetrachlorideHCID 24193—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-4-(4-chlorophenyl)pyrrolidin-3-amineHCID 6694061657%

Reaction Conditions

Temperature68 °C

Reaction Steps

Titanium (IV) chloride (0.36 g, 1.89 mmol) was added drop wise to a suspension of zinc powder (0.25 g, 3.78 mmol) in THF (3 ml). This solution was heated at 68° C. for one hour, then cooled to RT before (3SR,4RS)-1-benzyl-3-(4-chloro-phenyl)-4-nitro-pyrrolidine (0.20 g, 0.63 mmol) in THF (2 ml) was added. The reaction mixture was then stirred at reflux over night. The reaction was cooled to RT, diluted with 300 ml of Et2O, washed with an aqueous solution of NaHCO3 and the organic phases were dried over Na2SO4. Flash chromatography (SiO2, CH2Cl2/MeOH, 9:1) yielded 0.10 g (57%) of (3RS,4SR)-1-benzyl-4-(4-chloro-phenyl)-pyrrolidin-3-ylamine as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022099B2
Source datasetuspto-grants-2011_09
ORD IDord-9cc1570e8aa549d5b7452e677f85ca85
Source noteuspto-grants-2011_09