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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117634Generated: October 30, 2026

(4-Nitrophenyl)acetic acid → HCID 3522175, compound

https://huagongshe.com/reaction/2117634

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Nitrophenyl)acetic acidHCID 4661—
ReactantDichloromethaneHCID 6344—
ReactantThionyl ChlorideHCID 24386—
Reactant1-MethylpiperazineHCID 53167—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 3522175HCID 3522175—

Reaction Steps

4-Nitrophenylacetic acid (2.00 g, 0.011 mol) was dissolved in anhydrous THF (20 mL) with gradual addition of thionyl chloride (1.03 mL, 0.0143 mol) and a catalytic amount of DMF (2 drops) at room temperature and stirred for 24 h. On completion, the reaction was quenched in situ with N-methylpiperazine (3.85 g, 0.038 mol) added dropwise in a solution of DCM (20 mL) at room temperature and stirred overnight to give a beige suspension. The solvent was removed in vacuo and the residue partitioned between DCM (30 mL) and sodium hydroxide (1N, 30 mL). The organic layer was washed twice, dried over sodium sulfate and filtered. Removal of the solvent in vacuo the title compound as an amber oil, which solidified on standing. LCMS:2.5 min; Rt 0.82 (m/z 264, M+H+) 98%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442698B2
Source datasetuspto-grants-2008_10
ORD IDord-eb679a379c6d4c13a9db0e8f585e62ad
Source noteuspto-grants-2008_10