HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641598Generated: October 27, 2026
2-(Trifluoromethyl)aniline → N-(2-trifluoromethyl-phenyl)-malonamic acid benzyl ester
https://huagongshe.com/reaction/641598
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Trifluoromethyl)aniline | HCID 6922 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | Benzyl malonate | HCID 22247814 | — |
| Solvent | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Product | N-(2-trifluoromethyl-phenyl)-malonamic acid benzyl ester | HCID 68616692 | 57.6% |
Reaction Steps
A solution of mono-benzyl malonate (890 mg, 4.6 mmol) in 3:1 CH2Cl2/DMF (24 mL) was treated sequentially with N,N-diisopropylethylamine (2.0 mL, 11.5 mmol), 2-trifluoromethyl-phenylamine (0.6 mL, 4.6 mmol), and HATU (2.1 g, 5.5 mmol). The mixture was stirred for 12 h at RT, concentrated in vacuo, and partitioned between EtOAc and sat. NH4Cl. The aqueous phase was extracted with EtOAc (1×). The combined organic extracts were washed with sat. NaHCO3 and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified by flash chromatography to provide N-(2-trifluoromethyl-phenyl)-malonamic acid benzyl ester as an oil (894 mg, 57% yield). This material was dissolved in EtOAc (35 mL). The resultant solution was charged with 10% Pd/C (178 mg), stirred under H2 (1 atm) for 12 h at RT, filtered, and concentrated in vacuo to provide N-(2-trifluoromethyl-phenyl)-malonamic acid (621 mg, 95% yield). MS found: (M+H)+=248.02.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696205B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-51d288cbda5b421386b6491c109756ce |
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| Source note | uspto-grants-2010_04 |
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