HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724641Generated: October 30, 2026
Piperazine → 1-[2-(Methylsulphonyl)phenyl]piperazine
https://huagongshe.com/reaction/1724641
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Benzene, 1-bromo-2-(methylsulfonyl)- | HCID 190318 | — |
| Product | 1-[2-(Methylsulphonyl)phenyl]piperazine | HCID 11218677 | 34% |
Reaction Steps
A mixture of 2-bromo(methylsulfonyl)benzene (1.10 g, 4.7 mmol) and anhydrous piperazine (2.02 g, 23.5 mmol) was heated at 110° C. overnight. Then, the mixture was cooled and partitioned between 2 N NaOH and CH2Cl2. The separated organic layer was dried over Na2SO4 and concentrated under reduced pressure. The crude residue was chromatographed (CHCl3/CH3OH, 9:1, as eluent) to give 8 as a white semisolid (0.36 g, 34% yield). 1H NMR: δ 2.58 (s, 1H, NH, D2O exchanged), 2.84 (s, 4H, piperazinic), 3.14 (s, 3H, CH3), 7.10-7.83 (m, 4H, aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488730B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-f2fa2b6266a2460a97f9d62d6a21fa0a |
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| Source note | uspto-grants-2009_02 |
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