HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855513Generated: October 29, 2026
Cesium carbonate → 1-(3-Phenylsulfonylphenyl)-4-tert-butyloxycarbonylpiperazine
https://huagongshe.com/reaction/855513
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Benzene, 1-bromo-3-(phenylsulfonyl)- | HCID 640920 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(3-Phenylsulfonylphenyl)-4-tert-butyloxycarbonylpiperazine | HCID 68804741 | 71.2% |
Reaction Steps
A solution of 2 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP) (62 mg, 0.1 mmol) and cesium carbonate (329 mg, 1.01 mmol) in dry dioxane (2 ml) were sonicated for 45 min, under argon. To this solution was added 3-phenylsulfonylbromobenzene (D2) (200 mg, 0.67 mmol) and 1-(tert-butyloxycarbonyl)piperazine (314 mg, 1.68 mmol) and the reaction heated at 100° C. for 18 h. The reaction mixture was evaporated in vacuo and the residue partitioned between water (50 ml) and dichloromethane (50 ml). The organic layer was washed with sat. sodium hydrogen carbonate (50 ml), 10% citric acid (50 ml), brine (50 ml) and then dried (MgSO4). Solvents evaporated in vacuo and the residue purified by column chromatography (silica gel; 0-60% ethyl acetate/petroleum ether) to give the product as a colourless oil (192 mg, 71%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262188B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-ddeb902ce7a64ae688d3c01c150e46fa |
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| Source note | uspto-grants-2007_08 |
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