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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18900Generated: October 26, 2026

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

https://huagongshe.com/reaction/18900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPhenylacetyleneHCID 10821—
ReactantN-(2-benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamideHCID 3334757—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTriethylamineHCID 8471—
ProductN-(2-Benzoyl-4-chloro-phenyl)-4-phenylethynyl-benzenesulfonamideHCID 11328918—

Reaction Steps

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)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741519B2
Source datasetuspto-grants-2010_06
ORD IDord-903e7510157140739b126551ce0c9cd1
Source noteuspto-grants-2010_06