HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515007Generated: November 3, 2026
Dimethylformamide → 2,2,2-trifluoro-N-(4-formyl-3,5-dimethylphenyl)acetamide
https://huagongshe.com/reaction/1515007
Participants
| Role | Name | HCID | Charge |
|---|
| 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 | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | 2,2,2-trifluoro-N-(4-formyl-3,5-dimethylphenyl)acetamide | HCID 86632821 | — |
Reaction Steps
A solution of N-(4-bromo-3,5-dimethylphenyl)-2,2,2-trifluoroacetamide (14.0 g, 47.3 mmol) in THF (200 mL) was cooled to −78° C. Under a nitrogen atmosphere, methyllithium/LiBr (44.1 mL of a 1.5 M solution in Et2O, 66.2 mmol) was added slowly to the solution. After 5 min of stirring, sec-BuLi (47.3 mL of a 1.4 M solution in cyclohexane, 66.2 mmol) was added slowly to the reaction keeping the temperature at −78° C. After 5 min, anhydrous DMF (25.5 mL, 331 mmol) was added slowly to the solution. After the addition, the solution was warmed to 25° C. and after 30 min the reaction mixture was quenched with water. The aqueous layer was extracted with CH2Cl2 and the combined organic layers were washed with water, brine, dried with MgSO4 and filtered. The solvent was removed under reduced pressure to give 2,2,2-trifluoro-N-(4-formyl-3,5-dimethylphenyl)-acetamide as a yellow solid.
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-8af8b5fc928d45dfb98fdf63a3ce48cc |
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| Source note | uspto-grants-2012_07 |
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