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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859925Generated: October 26, 2026

Triphenylphosphine → 1-(Methylsulfonyl)-4-[4-(trimethylsilylethynyl)phenyl]piperazine

https://huagongshe.com/reaction/859925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant1-(4-Bromophenyl)-4-(methylsulfonyl)piperazineHCID 21919384—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventPiperidineHCID 8082—
Product1-(Methylsulfonyl)-4-[4-(trimethylsilylethynyl)phenyl]piperazineHCID 69606750—

Reaction Conditions

Temperature105 °C

Reaction Steps

To a stirred suspension of 1-(methylsulfonyl)-4-(4-bromophenyl)piperazine (4.79 g, 15 mmol, prepared as in example 3), trimethylsilylacetylene (4.15 mL, 30 mmol), Copper (I) iodide (31 mg, 0.17 mmol) and triphenylphosphine (80 mg, 0.3 mmol) in piperidine (60 mL) at 20° C. was added dichlorobis(triphenylphosphine)palladium(II) (31 mg, 45 μmol). The reaction was warmed to 105° C. and stirred for 8 hours under an inert atmosphere. After cooling, the suspension was filtered and washed with toluene. The solid was dissolved in CH2Cl2, washed with water and filtered through silica, washing with CH2Cl2. The filtrate was concentrated and the resulting suspension filtered, washing well with CH2Cl2/iHexane to give 1-(methylsulfonyl)-4-[4-(trimethylsilylethynyl)phenyl]piperazine as a white powder (3.05 g, 9.06 mmol, 60

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153857B2
Source datasetuspto-grants-2006_12
ORD IDord-ab3e761a5704466c90be9df35e415438
Source noteuspto-grants-2006_12