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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930526Generated: October 26, 2026

Potassium Carbonate → 1,3-Dimethyl-2-nitro-5-[1-(trifluoromethyl)vinyl]benzene

https://huagongshe.com/reaction/1930526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(3,3,3-Trifluoroprop-1-en-2-yl)boronic acidHCID 2782677—
Reactant5-Bromo-1,3-dimethyl-2-nitrobenzeneHCID 11958967—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1,3-Dimethyl-2-nitro-5-[1-(trifluoromethyl)vinyl]benzeneHCID 25100076105.1%

Reaction Steps

5-bromo-1,3-dimethyl-2-nitrobenzene (10.0 g), [1-(trifluoromethyl)vinyl]boronic acid (purity: 60%, 13.4 g) and potassium carbonate (14.4 g) was dissolved in the mixed solvent of THF and water, which was then degassed three times. To the solution was added dichloro bis(triphenylphosphine) palladium (II) (1.5 g), and the mixture was heated to reflux for 3 hours under argon atmosphere. The mixture was cooled to room temperature and then poured into water, which was then extracted twice with ethyl acetate. The organic layer was combined, which was then washed with water and dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the solvent was distilled away under the reduced pressure, and the residue was then purified by silica gel chromatography to yield 1,3-dimethyl-2-nitro-5-[1-(trifluoromethyl)vinyl]benzene (11.2 g). 1H-NMR (CDCl3) δ: 2.34 (6H, s), 5.78-5.80 (1H, m), 6.03-6.04 (1H, m), 7.20 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188122B2
Source datasetuspto-grants-2012_05
ORD IDord-c4a71be594cb4ad5baf83263c5fe03a0
Source noteuspto-grants-2012_05