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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483186Generated: November 1, 2026

Potassium Carbonate → 4-Bromo-3,5-dimethylphenyl 3-(3-nitrophenyl)propiolate

https://huagongshe.com/reaction/1483186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Iodo-3-nitrobenzeneHCID 12574—
Reactant4-Bromo-3,5-dimethylphenyl propiolateHCID 72545233—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-3,5-dimethylphenyl 3-(3-nitrophenyl)propiolateHCID 8947776529%

Reaction Conditions

Temperature65 °C

Reaction Steps

1-Iodo-3-nitrobenzene (41.05 g, 164.3 mmol) in THF (100 mL) was degassed under reduced pressure at −78° C., and then nitrogen gas was introduced. To the solution was added K2CO3 (41.27 g, 298.6 mmol), CuI (2.27 g, 11.9 mmol) and PdCl2(Ph3P)2 (1.11 g, 1.57 mmol), and the mixture was stirred at 65° C. 4-bromo-3,5-dimethylphenyl propiolate (6-1) (37.79 g, 149.3 mmol) in THF (68 mL) was added by syringe pump over a period of 5.4 hr, and the mixture was stirred an additional 1 h after addition was complete. After being cooled to room temperature, the mixture was filtered. The filtrate was concentrated and purified by silica gel column chromatography. The fractions containing the desired compound were concentrated. To the concentrate added hexane and the precipitated solid was collected by filtration. The solid was washed with hexane and dried to give the title compound 6-2 (15.96 g, 29% yield) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416121B2
Source datasetuspto-grants-2016_08
ORD IDord-6dbdfa8f095c4178bdd62a44f2c4d7f3
Source noteuspto-grants-2016_08