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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992046Generated: October 30, 2026

1-Fluoro-2-nitrobenzene → 8-Benzyl-N-(2-nitrophenyl)-8-azabicyclo[3.2.1]octan-3-amine

https://huagongshe.com/reaction/1992046

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantDiisopropylethylamineHCID 81531—
Reactant8-Benzyl-8-azabicyclo(3.2.1)octan-3-amineHCID 12832103—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product8-Benzyl-N-(2-nitrophenyl)-8-azabicyclo[3.2.1]octan-3-amineHCID 1850702631.1%

Reaction Steps

5.62 g (27.82 mmol) 8-benzyl-8-azabicyclo[3.2.1]octan-3-amine (u17094-94) and 9.7 ml (55.46 mmoml) of Hunig's base were dissolved in 200 ml NMP. 4.32 g (30.60 mmol) 1-fluoro-2-nitrobenzene was then added and the mixture was stirred at RT for 3 hrs. The reaction mixture was diluted with EtOAc and washed with water and dried over sodium sulfate. The solvent was removed partially under reduced pressure and was left in refrigerator overnight. The solid was filtered off to afford 2.92 g of product as a yellow powder. The solvent was removed from filtration to give additional 5.7 g of product as an orange-yellow residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645771B2
Source datasetuspto-grants-2010_01
ORD IDord-05b846e7297742f39ca0abff504cb597
Source noteuspto-grants-2010_01