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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365852Generated: October 31, 2026

Pyrrolidine → HCID 66937954, compound

https://huagongshe.com/reaction/1365852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant1,4-DioxaneHCID 31275—
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant1-Bromo-5-fluoro-2-methyl-3-nitrobenzeneHCID 2773385—
ProductHCID 66937954HCID 66937954—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 1-bromo-5-fluoro-2-methyl-3-nitro-benzene (7.49 g, 31.8 mmol) in dioxane (40 mL) were added DMF-DMA (21.0 mL, 158 mmol) and pyrrolidine (2.6 mL, 31.1 mmol). The reaction mixture was heated at 100° C. for 3 h. The mixture was cooled to RT and concentrated in vacuo to give 1-[2-(2-bromo-4-fluoro-6-nitro-phenyl)-1-methyl vinyl]-pyrrolidine as a dark red residue. To a suspension of the pyrrolidine (10.0 g, 31.7 mmol) and Raney®-Nickel (suspension in H2O, 15 mL) in MeOH:THF (1:1, 150 mL) was added hydrazine monohydrate (2.3 mL, 47.4 mmol) at 0° C. and the mixture stirred at RT for 5 hours. The reaction mixture was then filtered through Celite and the filter cake washed with EtOAc. The filtrate was concentrated in vacuo and the resulting residue was purified by column chromatography (silica gel, pentane:EtOAc 75:25) to provide the title compound as a pale oil (2.57 g, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893060B2
Source datasetuspto-grants-2011_02
ORD IDord-297f4ed9a55a48559d4fbd735294060f
Source noteuspto-grants-2011_02