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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-[4-(2,2,2-Trifluoroethoxy)phenyl]piperazineHCID 43510344—
SolventDichloromethaneHCID 6344—
Product1-(Methylsulfonyl)-4-[4-(2,2,2-trifluoroethoxy)phenyl]piperazineHCID 2106862419.5%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485644B2
Source datasetuspto-grants-2009_02
ORD IDord-0c7223e91e814e678a6c46b4b906b5a2
Source noteuspto-grants-2009_02