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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325227Generated: October 25, 2026

Diethylamine → (4-Ethynyl-2-phenylbenzoyl)methionine methyl ester

https://huagongshe.com/reaction/325227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(2-Phenyl4bromobenzoyl)-methionine methyl esterHCID 20622824—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystPalladium(2+) acetate--triphenylphosphane (1/2/2)HCID 84538—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product(4-Ethynyl-2-phenylbenzoyl)methionine methyl esterHCID 54338681—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of (2-phenyl-4-bromobenzoyl)-methionine methyl ester (100 mmol), diethylamine (300 mmol), trimethylsilylacetylene (110 mmol), bis(triphenylphosphine) palladium diacetate (5 mmol) and copper(I) iodide (3 mmol) in toluene is heated at 60° C. until TLC analysis indicates the starting methyl ester has disappeared. The reaction mixture is concentrated in vacuo, redissolved in ether, filtered through silica gel, and concentrated. The residue is then dissolved in THF, and is treated with tetrabutylammonium fluoride (120 mmol). After TLC analysis indicates that no starting material is left, the reaction mixture is diluted with ether, washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue is then purified with column chromatography on silica gel to give the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06221865B1
Source datasetuspto-grants-2001_04
ORD IDord-b1295a32a5004ca08bcd2230412b11eb
Source noteuspto-grants-2001_04