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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 1-(4-Bromophenyl)-4-(methylsulfonyl)piperazine | HCID 21919384 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Piperidine | HCID 8082 | — |
| Product | 1-(Methylsulfonyl)-4-[4-(trimethylsilylethynyl)phenyl]piperazine | HCID 69606750 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153857B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-ab3e761a5704466c90be9df35e415438 |
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| Source note | uspto-grants-2006_12 |
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