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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365910Generated: November 2, 2026

rac-(3R,4S)-1-Benzyl-3-(4-fluoro-phenyl)-4-nitro-pyrrolidine → 1-Benzyl-4-(4-fluorophenyl)pyrrolidin-3-amine

https://huagongshe.com/reaction/1365910

Reaction equation

Participants

RoleNameHCIDCharge
Reactantrac-(3R,4S)-1-Benzyl-3-(4-fluoro-phenyl)-4-nitro-pyrrolidineHCID 66940721—
CatalystZincHCID 23994—
CatalystTitanium TetrachlorideHCID 24193—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-4-(4-fluorophenyl)pyrrolidin-3-amineHCID 6694092622.6%

Reaction Conditions

Temperature68 °C

Reaction Steps

Titanium (IV) chloride (179.4 g, 0.94 mol) was added drop wise to a suspension of zinc powder (123.6 g, 1.89 mol) in THF (1200 ml). This solution was heated at 68° C. for one hour, then cooled to RT before rac-(3R,4S)-1-benzyl-3-(4-fluoro-phenyl)-4-nitro-pyrrolidine (94 g, 0.31 mol) in THF (400 ml) was added. The reaction mixture was then stirred at reflux over night. The reaction was cooled to RT, diluted with 3000 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 18.9 g (22%) of rac-(3S,4R)-1-benzyl-4-(4-fluoro-phenyl)-pyrrolidin-3-ylamine as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893062B2
Source datasetuspto-grants-2011_02
ORD IDord-9582d1c795d94db5a74cf860bac88832
Source noteuspto-grants-2011_02