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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978192Generated: October 28, 2026

N,N-Dimethylpropargylamine → 2-Chloro-4-(3-dimethylaminopropyn-1-yl)-benzoic acid methyl ester

https://huagongshe.com/reaction/1978192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylpropargylamineHCID 81643—
ReactantMethyl 4-Bromo-2-chlorobenzoateHCID 22058730—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product2-Chloro-4-(3-dimethylaminopropyn-1-yl)-benzoic acid methyl esterHCID 5397928493.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

Under an atmosphere of nitrogen, a mixture of 4-bromo-2-chlorobenzoic acid methyl ester (25.13 g, 101 mmol), 1-dimethylamino-2-propyne (16 mL, 150 mmol), bis(triphenylphosphine)palladium(II) chloride (1.0 g) and copper (I) iodide (0.15 g) in 100 mL of triethylamine was heated at 60° C. for 2 hours. The cooled reaction mixture was filtered through Solka floc and the cake was washed with ethyl acetate. The filtrate was partitioned between ethyl acetate and dilute aqueous sodium thiosulfate. The organic layer was washed with water, brine and dried over sodium sulfate. The dark solution was filtered through a plug of Merck-60 silica gel and the filtrate was concentrated in vacuo to give the title compound (23.8 g) as an orange oil, which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235900B1
Source datasetuspto-grants-2001_05
ORD IDord-1aca30fc979647a581c03f7db961e3db
Source noteuspto-grants-2001_05