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HRID 1765527作成日:2026年10月25日

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

https://huagongshe.com/reaction/1765527

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物1,2-DimethoxyethaneHCID 8071—
反応物PhenylacetyleneHCID 10821—
反応物N-(2-benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamideHCID 3334757—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒TriethylamineHCID 8471—
生成物N-(2-Benzoyl-4-chloro-phenyl)-4-phenylethynyl-benzenesulfonamideHCID 11328918—

反応手順

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 (MgSO4), 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07227035B2
出典データセットuspto-grants-2007_06
ORD IDord-a558f353168040449fb18fc3c4c1d9ea
出典メモuspto-grants-2007_06