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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodo-3-nitrobenzene | HCID 12574 | — |
| Reactant | 4-Bromo-3,5-dimethylphenyl propiolate | HCID 72545233 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Bromo-3,5-dimethylphenyl 3-(3-nitrophenyl)propiolate | HCID 89477765 | 29% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09416121B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-6dbdfa8f095c4178bdd62a44f2c4d7f3 |
|---|
| Source note | uspto-grants-2016_08 |
|---|