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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487150Generated: October 30, 2026

Benzoyl chloride, 3-nitro- → (4-Methylpiperazin-1-yl)(3-nitrophenyl)methanone

https://huagongshe.com/reaction/1487150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-nitro-HCID 8495—
Reactant1-MethylpiperazineHCID 53167—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(4-Methylpiperazin-1-yl)(3-nitrophenyl)methanoneHCID 76341186%

Reaction Steps

To a solution of 3-nitrobenzoyl chloride (4.5 g, 24.25 mmol) in THF (30 ml) was added 1-methylpiperazine (8.50 g, 85 mmol). The reaction was stirred for 20 min at room temperature. The reaction mixture was diluted with 50 mL water and extracted with ethyl acetate (2×100 mL). The combined organic layer was washed with brine (50 mL). The brine was back extracted with ethyl acetate (2×50 mL) and all the organic layers were combined, dried over magnesium sulphate, filtered, and concentrated under vacuum give the title product (5.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428499B2
Source datasetuspto-grants-2016_08
ORD IDord-527177e999374add81098adf56dd4054
Source noteuspto-grants-2016_08