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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360771Generated: November 1, 2026

Dimethylformamide → 2,2,2-trifluoro-N-(4-formyl-3,5-dimethylphenyl)acetamide

https://huagongshe.com/reaction/1360771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantN-(4-bromo-3,5-dimethylphenyl)-2,2,2-trifluoroacetamideHCID 21336351—
ReactantCID 53628100HCID 178418400—
ReactantHCID 178419607HCID 178419607—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
Product2,2,2-trifluoro-N-(4-formyl-3,5-dimethylphenyl)acetamideHCID 86632821—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of N-(4-bromo-3,5-dimethylphenyl)-2,2,2-trifluoroacetamide (U.S. Pat. No. 6,391,865) (14.0 g. 47.3 mmol) in THF (200 mL) under nitrogen atmosphere at −78° C. was added slowly methyllithium/LiBr (44.1 mL of a 1.5 M solution in Et2O, 66.2 mmol). 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 solution at −78° C. After 5 min, anhydrous DMF (25.5 mL, 331 mmol) was added slowly then the solution was warmed to 25° C. 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 over MgSO4 and filtered. The solvent was removed under reduced pressure to give the title compound as a yellow solid. MS: m/z 246 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879850B2
Source datasetuspto-grants-2011_02
ORD IDord-2b8037a6960048a58faaa0146acf5adf
Source noteuspto-grants-2011_02