Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238133Generated: October 25, 2026

Potassium Carbonate → 1-(Cyclopropanesulfonimidoyl)-4-nitrobenzene

https://huagongshe.com/reaction/238133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTrifluoroacetamideHCID 67717—
ReactantMagnesium monoxideHCID 6850729—
ReactantIodo benzene diacetateHCID 12217721—
Reactant1-(Cyclopropanesulfinyl)-4-nitrobenzeneHCID 59550834—
CatalystDirhodium tetraacetateHCID 152122—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(Cyclopropanesulfonimidoyl)-4-nitrobenzeneHCID 56949253—

Reaction Steps

6.6 g (31.24 mmol) (RS)-1-(cyclopropylsulfinyl)-4-nitrobenzene, 7.77 g trifluoroacetamide (68.74 mmol), 16.6 g (51.55 mmol) iodobenzene diacetate and 5.54 g (137.5 mmol) magnesium oxide are placed in 350 ml dichloro-methane. The mixture is stirred for 5 minutes, treated with 0.69 g (1.56 mmol) rhodium(II) acetate dimer and stirred at room temperature for 12 hours. The suspension is diluted with 235 ml methanol, treated with 23.75 g potassium carbonate and stirred at room temperature for 4 hours. Next the mixture is treated with 400 ml water, and the organic phase is separated and filtered at the pump through Celite®. The aqueous phase is extracted several times with dichloromethane. The combined organic phases are washed with half-saturated sodium chloride solution and stirred with 100 ml 2N hydrochloric acid for 30 minutes. The aqueous phase is adjusted to pH 9 with concentrated sodium hydroxide solution with ice cooling. The crystallised product is aspirated dry, washed with water and dried. 4.7 g (66.5% of theor.) of the product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642611B2
Source datasetuspto-grants-2014_02
ORD IDord-316d629c237c41b6b05d4e126ba5b725
Source noteuspto-grants-2014_02