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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713790Generated: October 27, 2026

Benzene, 1-fluoro-2-methyl-4-nitro- → 1-Acetyl-4-(2-methyl-4-nitrophenyl)piperazine

https://huagongshe.com/reaction/1713790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-fluoro-2-methyl-4-nitro-HCID 68001—
Reactant1-AcetylpiperazineHCID 83795—
Reactant1-Butyl-3-methylimidazolium hexafluorophosphateHCID 2734174—
SolventAcetonitrileHCID 6342—
Product1-Acetyl-4-(2-methyl-4-nitrophenyl)piperazineHCID 5303057—

Reaction Conditions

Temperature85 °C

Reaction Steps

1-Butyl-3-methylimidazolium hexafluorophosphate (1.75 g, 7.7 mmol) and acetyl piperazine (39.7 g, 309.4 mmol) was added to a stirred solution of 2-fluoro-5-nitrotoluene (12 g, 77.4 mmol) in MeCN (3 mL) and heated to 85° C. for 2 h. The reaction was cooled and concentrated in vacuo. Water (100 mL) was added to the resulting residue and the reaction extracted with EtOAc (3×100 mL). The solvent was dried (MgSO4), filtered, and concentrated in vacuo to yield the product as a yellow solid which was triturated with isohexane and dried in vacuo at 60° C.; 1H NMR δ 8.05 (2H, m), 7.14 (1H, d), 3.64-3.58 (4H, m), 3.05-2.94 (4H, m), 2.37 (3H, s), 2.37 (3H, s); MS m/e MH+ 264.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795283B2
Source datasetuspto-grants-2010_09
ORD IDord-15ead006b72044e7ac3178e63cba7ace
Source noteuspto-grants-2010_09