HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040389Generated: October 27, 2026
Dimethylamine → 4-(Dimethylamino)-2-(trifluoromethyl)benzaldehyde
https://huagongshe.com/reaction/1040389
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluoro-2-(trifluoromethyl)benzaldehyde | HCID 522940 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Dimethylamino)-2-(trifluoromethyl)benzaldehyde | HCID 71372892 | 70% |
Reaction Steps
A suspension of 4-fluoro-2-trifluoromethylbenzaldehyde (500 mg, 2.60 mmol), dimethylamine (5.5 mol/L in ethanol, 0.95 mL, 5.2 mmol), potassium carbonate (360 mg, 2.6 mmol) in 5.2 mL of N,N-dimethylformamide was stirred at 110° C. overnight in a sealed tube. After the reaction mixture was diluted with water, the solution was extracted with ether. The extract was washed with brine, and dried over MgSO4. After filtration, the filtrate was concentrated in vacuo, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=85/15 to 75/25) to obtain the title compound as a pale yellow powder (393 mg, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552220B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-47696a39f748424c8358cbf8292945b0 |
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| Source note | uspto-grants-2013_10 |
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