HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912864Generated: October 31, 2026
Potassium Carbonate → 4-(4-methylpiperazin-1-yl)-3-(trifluoromethyl)aniline
https://huagongshe.com/reaction/1912864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2-Fluoro-5-nitrobenzotrifluoride | HCID 94954 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-methylpiperazin-1-yl)-3-(trifluoromethyl)aniline | HCID 6500400 | 94% |
Reaction Steps
In 10 mL of dimethylformamide, 300 mg (1.44 mmol) of 2-fluoro-5-nitrobenzotrifluoride was dissolved, and 287 mg (2.88 mmol) of 4-methylpiperazine and 792 mg (5.76 mmol) of potassium carbonate were added thereto and the mixture solution was heated at 70° C. for three hours with vigorous stirring. After cooling, the reaction solution was poured into a saturated sodium bicarbonate solution and extracted with ethyl acetate, and the extract was washed with a saturated sodium chloride solution, and the obtained organic layer as such was used as a substrate in the subsequent catalytic reduction. To the organic layer, 10 mg of 10% palladium carbon was added and the mixture was stirred at room temperature for 16 hours in a hydrogen atmosphere at normal pressures. The catalyst was removed by filtration and the filtrate was concentrated and purified by silica gel column chromatography to obtain 350 mg (94%) of a target product as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609656B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-e26a90c1e3ea42dcad80ad25d4d088cf |
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| Source note | uspto-grants-2013_12 |
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