Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantBinap, (A+-)-HCID 634876—
ReactantBenzene, 1-bromo-3-(phenylsulfonyl)-HCID 640920—
Solvent1,4-DioxaneHCID 31275—
Product1-(3-Phenylsulfonylphenyl)-4-tert-butyloxycarbonylpiperazineHCID 6880474171.2%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262188B2
Source datasetuspto-grants-2007_08
ORD IDord-ddeb902ce7a64ae688d3c01c150e46fa
Source noteuspto-grants-2007_08