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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-(4-Methylpiperazin-1-yl)phenyl acetate | HCID 67973796 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Bromo-4-(4-methylpiperazin-1-yl)phenyl acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541576B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-c784f788c35a4ab4831870a108a1a15f |
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| Source note | uspto-grants-2013_09 |
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