HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723826Generated: October 25, 2026
Triethylamine → 1-(Methylsulfonyl)-4-[4-(2,2,2-trifluoroethoxy)phenyl]piperazine
https://huagongshe.com/reaction/1723826
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-[4-(2,2,2-Trifluoroethoxy)phenyl]piperazine | HCID 43510344 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Methylsulfonyl)-4-[4-(2,2,2-trifluoroethoxy)phenyl]piperazine | HCID 21068624 | 19.5% |
Reaction Steps
1-[4-(2,2,2-trifluoroethoxy)phenyl]piperazine (13.48 g, 50 mmol) was dissolved in DCM (500 mL) and cooled to 0° C. Triethylamine (29 mL, 0.2 mol) was added, followed by the dropwise addition of methanesulfonyl chloride (4.2 mL, 55 mmol). The reaction was then allowed to warm to room temperature and stir overnight, before being quenched by the addition of water. The layers were separated, and the organic phase dried (MgSO4), filtered and concentrated. The residue was recrystallised from hot ethanol to give pure 1-(methylsulfonyl)-4-[4-(2,2,2-trifluoroethoxy)phenyl]piperazine (3.3 g, 18%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07485644B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-0c7223e91e814e678a6c46b4b906b5a2 |
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| Source note | uspto-grants-2009_02 |
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