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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365908Generated: 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/1365908

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 rac-(3R,4S)-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 rac-(3S,4R)-1-benzyl-4-(4-chloro-phenyl)-pyrrolidin-3-ylamine as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893062B2
Source datasetuspto-grants-2011_02
ORD IDord-7a42690f6c8447908ddbbfb277c55aa4
Source noteuspto-grants-2011_02