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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261916Generated: November 4, 2026

Acetone → Benzamide

https://huagongshe.com/reaction/2261916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDiisopropylamineHCID 7912—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant3-bromo-N-[(1R)-1-(4-fluorophenyl)ethyl]-5-[methyl(methylsulfonyl)amino]benzamideHCID 58990084—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystBis(tri-tert-butylphosphine)palladium(0)HCID 2734558—
CatalystDipalladium chloroformHCID 86615680—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductBenzamideHCID 2331—

Reaction Steps

To a solution of 3-(N-methyl-N-(methylsulfonyl)amino)-5-bromo-N—((R)-1-(4-fluorophenyl)ethyl)benzamide (200 mg, 0.46 mmol), copper(I)iodide (3.6 mg, 0.019 mmol), bis(tri-t-butylphosphine) palladium (0) (14 mg, 0.028 mmol) and tris(dibenzylide acetone) dipalladium (0) chloroform adduct (14.2 mg, 0.014 mmol) in 0.5 mL degassed dioxane was added diisopropylamine (0.084 mL, 0.60 mmol) and (trimethylsilyl)acetylene (0.085 mL, 0.60 mmol). The reaction was stirred at rt overnight and then heated to 60° C. for an additional night. The mixture was diluted with EtOAc and filtered through celite. Concentration and flash chromatography (10-50% EtOAc/hexanes) gave 3-(N-methyl-N-(methylsulfonyl)amino)-N—((R)-1-(4-fluorophenyl)ethyl)-5-(2-trimethylsilyl)ethynyl)benzamide. 1H NMR (CDCl3) δ 7.77 (m, 1H), 7.67 (m, 1H), 7.61 (m, 1H), 7.35 (m, 2H), 7.05 (m, 2H), 6.28 (d, J=7.3 Hz, 1H), 5.29 (m, 1H), 3.33 (s, 3H), 2.86 (s, 3H), 1.60 (d, J=7.0 Hz, 3H), 0.26 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07847100B2
Source datasetuspto-grants-2010_12
ORD IDord-7b841ceb63f14939821050a35721ec06
Source noteuspto-grants-2010_12