HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514976Generated: November 1, 2026
Dimethylformamide → 2,2,2-trifluoro-N-(4-formyl-3,5-dimethylphenyl)acetamide
https://huagongshe.com/reaction/1514976
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-(4-bromo-3,5-dimethylphenyl)-2,2,2-trifluoroacetamide | HCID 21336351 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Reactant | HCID 178419607 | HCID 178419607 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,2,2-trifluoro-N-(4-formyl-3,5-dimethylphenyl)acetamide | HCID 86632821 | — |
Reaction Steps
To a solution of N-(4-bromo-3,5-dimethylphenyl)-2,2,2-trifluoroacetamide (592 mg) in THF (10 mL) at −78° C. was added MeLi/LiBr (1.5M in Et2O, 1.87 mL) slowly. After 5 min, sec-BuLi (1.4M. in cyclohexane, 2.0 mL) was added slowly to the solution at −78° C. After 5 min DMF (0.31 mL) was added to the solution drowise at −78° C. then the mixture was warmed to room temperature. After 30 min the reaction mixture was partioned between water and CH2Cl2. The aqueous layer was extracted with CH2Cl2 and the combined organic layers were dried and filtered. Removal of the solvent under reduced pressure to gave a yellow solid which was purified by flash chromatography using hexanes/ethyl acetate (5:1) as eluent which gave 2,2,2-trifluoro-N-(4-formyl-3,5-dimethyl-phenyl)-acetamide as a light yellow solid. MS (ESI)m/z 246 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222248B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-a85e9f62c9ab44edb837f092b1fde15e |
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| Source note | uspto-grants-2012_07 |
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