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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723681Generated: November 3, 2026

Diisopropylamine → 2-(2-Chlorophenylamino)-3,4-difluoro-6-trimethylsilanylethynylbenzoic acid methyl ester

https://huagongshe.com/reaction/1723681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant6-Bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid methyl esterHCID 86598592—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Chlorophenylamino)-3,4-difluoro-6-trimethylsilanylethynylbenzoic acid methyl esterHCID 8659859379%

Reaction Steps

A mixture of 6-bromo-2-(2-chlorophenylamino)-3,4-difluorobenzoic acid methyl ester (2.61 g, 6.93 mmol), TMS-acetylene (1.18 mL, 8.32 mmol), Pd(PPh3)2Cl2 (496 mg, 0.693 mmol), CuI (132 mg, 0.693 mmol), and i-Pr2NH (1.95 mL, 13.9 mmol) in THF (11 mL) was stirred for 16 hours at room temperature. The reaction mixture was concentrated in vacuo, diluted with EtOAc, and washed with saturated aqueous NH4Cl and brine. The organic layer was dried over MgSO4, filtered, and concentrated to give the crude material that was purified by silica gel flash column chromatography (100% hexanes to 1% to 2% EtOAc in hexanes) to afford the desired product (2.15 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485643B2
Source datasetuspto-grants-2009_02
ORD IDord-a9b26cc0fdfc4ec18e9feb4226bbfb3d
Source noteuspto-grants-2009_02