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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45808Generated: October 25, 2026

p-Toluenesulfonic acid → 2-Bromo-4-(4-methylpiperazin-1-yl)phenyl acetate

https://huagongshe.com/reaction/45808

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantBromineHCID 24408—
Reactant4-(4-Methylpiperazin-1-yl)phenyl acetateHCID 67973796—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-Bromo-4-(4-methylpiperazin-1-yl)phenyl acetateHCID 67973664—

Reaction Steps

A solution of 4-(4-methylpiperazin-1-yl)phenyl acetate 247 mg (1.05 mmol) and p-toluenesulfonic acid 209 mg (1.1 mmol) in acetonitrile was cooled in an ice bath and bromine 0.056 ml (1.1 mmol) was added dropwise. The reaction was stirred at room temperature until complete (3-4 hours), was diluted with ethyl acetate and extracted with water and saturated NaHCO3. The organic phase, dried over Na2SO4 and evaporated, was purified by flash chromatography (DCM/MeOH 85/15) to give the product as a dark brown oil. HPLC (254 nm) method 2 Rt 4.05 min. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.25 (s, 3H) 2.36 (s, 3H) 2.39 (m, 4H) 3.44 (m, 4H) 6.50 (dd. J=2.1, 8.3 Hz, 1H) 7.03 (d, J=8.3 Hz, 1H) 7.21 (d, J=2.1 Hz, 1H). Mass. Calc. 313.0546 Mass. Found: 313.0538

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541576B2
Source datasetuspto-grants-2013_09
ORD IDord-c784f788c35a4ab4831870a108a1a15f
Source noteuspto-grants-2013_09