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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161864Generated: October 28, 2026

(Diethylamino)sulfur trifluoride → 1,4-Dibenzyl-2-(fluoromethyl)piperazine

https://huagongshe.com/reaction/1161864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
Reactant(1,4-Dibenzylpiperazin-2-yl)methanolHCID 10827800—
SolventDichloromethaneHCID 6344—
Product1,4-Dibenzyl-2-(fluoromethyl)piperazineHCID 1447949940%

Reaction Conditions

Temperature-78 °C

Reaction Steps

(1,4-Dibenzylpiperazin-2-yl)methanol (15 g, 50.5 mmol) in DCM (50 mL) was added dropwise to a stirred solution of DAST (7.42 mL, 60.6 mmol) in DCM (150 mL) cooled to −78° C. The reaction mixture was maintained below −30° C. for 24 h before warming to room temperature and stirring for an additional 20 h. The reaction was quenched by the addition of water (100 mL). The organic phase was separated, the aqueous basified with NaOH (aq.) to pH 10 and extracted with DCM (3×75 mL). The combined organics were washed with water (2×100 mL), brine (2×100 mL), dried (Na2SO4) and concentrated under reduced pressure. The resultant oil was purified by chromatography on silica gel with EtOAc:heptane (1:9, v/v) as eluent to afford 1,4-dibenzyl-2-fluoromethylpiperazine (6.0 g, 20.1 mmol, 40%). A biproduct of the reaction was also isolated, 1,4-dibenzyl-6-fluoroperhydro-1,4-diazepine (1.0 g, 3.35 mmol, 7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820649B2
Source datasetuspto-grants-2010_10
ORD IDord-c074c48f39ec4938a83c1f9a55474c83
Source noteuspto-grants-2010_10