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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78321생성일: 2026년 10월 25일

Phenol → 4-(3-(N-methylsulfamoyl)phenyloxy)benzene

https://huagongshe.com/reaction/78321

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물Potassium CarbonateHCID 11430—
반응물3-bromo-N-methylbenzene-1-sulfonamideHCID 7213265—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DimethylformamideHCID 6228—
생성물4-(3-(N-methylsulfamoyl)phenyloxy)benzeneHCID 2361457311.4%

반응 단계

To a slurry of phenol (1.9 g, 20 mmol), K2CO3 (6.0 g, 40 mmol), and CuI (4 g, 20 mmol) in DMF (25 mL) was added N-methyl-3-bromobenzenesulfonamide (2.5 g, 10 mmol), and the resulting mixture was stirred at the reflux temp. overnight, cooled to room temp., and separated between EtOAc (50 mL) and a 1 N HCl solution (50 mL). The aqueous layer was back-extracted with EtOAc (2×50 mL). The combined organic phases were sequentially washed with water (2×50 mL) and a saturated NaCl solution (50 mL), dried (MgSO4), and concentrated under reduced pressure. The residual oil was purified by column chromatography (30% EtOAc/70% hexane) to give 4-(3-(N-methylsulfamoyl)phenyloxy)benzene (0.30 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841330B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-06ae73dc4a0c43308c9126c1333fa8b9
출처 메모uspto-grants-2014_09