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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylpropargylamine | HCID 81643 | — |
| Reactant | Methyl 4-Bromo-2-chlorobenzoate | HCID 22058730 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-Chloro-4-(3-dimethylaminopropyn-1-yl)-benzoic acid methyl ester | HCID 53979284 | 93.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06235900B1 |
|---|
| Source dataset | uspto-grants-2001_05 |
|---|
| ORD ID | ord-1aca30fc979647a581c03f7db961e3db |
|---|
| Source note | uspto-grants-2001_05 |
|---|