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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

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

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222248B2
Source datasetuspto-grants-2012_07
ORD IDord-8af8b5fc928d45dfb98fdf63a3ce48cc
Source noteuspto-grants-2012_07