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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190863Generated: October 31, 2026

1-Methylpiperazine → [2-(4-Methylpiperazino)-5-nitrophenyl]methanol

https://huagongshe.com/reaction/1190863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant(2-Fluoro-5-nitrophenyl)methanolHCID 4437169—
SolventTetrahydrofuranHCID 8028—
Product[2-(4-Methylpiperazino)-5-nitrophenyl]methanolHCID 2591881294%

Reaction Steps

2-Fluoro-5-nitrobenzyl alcohol (1 g, 5.84 mmol) and N-methylpiperazine (1.29 mL, 2 eq) were heated at 130° C. for 1 h. The reaction mixture was then diluted with 25 mL of THF and washed with a saturated aqueous solution of Na2CO3 and then with brine. The organic layer was dried over Na2SO4, filtered and evaporated. The residue was thoroughly washed with pentane and filtered off to yield expected compound as an orange powder (1.38 g, 94% yield). m/z (ESI) 252.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680095B2
Source datasetuspto-grants-2014_03
ORD IDord-a7a4d715d5a94319bcd29bd81c8f21d4
Source noteuspto-grants-2014_03