돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238133생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/238133

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물TrifluoroacetamideHCID 67717—
반응물Magnesium monoxideHCID 6850729—
반응물Iodo benzene diacetateHCID 12217721—
반응물1-(Cyclopropanesulfinyl)-4-nitrobenzeneHCID 59550834—
촉매Dirhodium tetraacetateHCID 152122—
용매MethanolHCID 887—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물1-(Cyclopropanesulfonimidoyl)-4-nitrobenzeneHCID 56949253—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642611B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-316d629c237c41b6b05d4e126ba5b725
출처 메모uspto-grants-2014_02