HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874780Generated: October 25, 2026
Potassium Carbonate → 1,3-Dimethyl-2-nitro-5-[1-(trifluoromethyl)vinyl]benzene
https://huagongshe.com/reaction/874780
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3,3,3-Trifluoroprop-1-en-2-yl)boronic acid | HCID 2782677 | — |
| Reactant | 5-Bromo-1,3-dimethyl-2-nitrobenzene | HCID 11958967 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Dimethyl-2-nitro-5-[1-(trifluoromethyl)vinyl]benzene | HCID 25100076 | 105.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980937B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-00c71b5c0d99490389df89743c33366b |
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| Source note | uspto-grants-2015_03 |
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