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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239847생성일: 2026년 10월 25일

Dichloromethane → N-(2-Benzoyl-4-chloro-phenyl)-4-phenylethynyl-benzenesulfonamide

https://huagongshe.com/reaction/239847

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물1,2-DimethoxyethaneHCID 8071—
반응물PhenylacetyleneHCID 10821—
반응물N-(2-benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamideHCID 3334757—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Tetrabutylammonium IodideHCID 67553—
용매TriethylamineHCID 8471—
생성물N-(2-Benzoyl-4-chloro-phenyl)-4-phenylethynyl-benzenesulfonamideHCID 11328918—

반응 단계

To a magnetically stirred mixture of the N-(2-Benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamide (450 mg, 1.0 mmol), [1,1′ Bis-(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (1:1) (30 mg, 0.037 mmol) and copper (I) iodide (100 mg, 0.52 mmol) was added DME (6 mL) and dry triethylamine (3 mL) under dry nitrogen. To this stirred mixture was added tetrabutylammonium iodide (250 mg), followed by the addition of phenylacetylene (0.240 mL). The dark green mixture was stirred at ambient temp overnight. The reaction was worked up by addition to crushed ice and extracted with ethyl acetate (3×75 mL), and the organic layer was dried (MgSC4), filtered and concentrated. The crude product was chromatographed on silica gel using 10-30% EtOAc/Hexane. 1H NMR (CDCl3) δ 9.64 (br s, 1H, NH), 7.75 (d, 1H, J=Hz), 7.75 (d, 1H, J=8.8 Hz), 7.48 (m, 8H), 7.36 (m, 7H). MS: m/z 472 (M+1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642808B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-8063ddaf989144d4a772fce440c3c85f
출처 메모uspto-grants-2014_02