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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188484Generated: October 31, 2026

N-[4-chloro-2-methyl-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamide → N-(4-cyano-2-methyl-3-(trifluoromethyl)phenyl)pivalamide

https://huagongshe.com/reaction/1188484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-chloro-2-methyl-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamideHCID 21874848—
ReactantHCID 178418260HCID 178418260—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-(4-cyano-2-methyl-3-(trifluoromethyl)phenyl)pivalamideHCID 2187502089.2%

Reaction Conditions

Temperature200 °C

Reaction Steps

A solution of N-[4-chloro-2-methyl-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamide (0.257 g, 0.875 mmol) in NMP (2.5 mL) was treated with copper cyanide (0.180 g, 2.01 mmol) and the resulting suspension was heated to 200° C. in a microwave for 14 h. The cooled reaction mixture was diluted with EtOAc and water and then filtered through a pad of celite. The filtrate was concentrated to a brown oil and then partitioned between Et2O and water. The aqueous portion was further extracted with Et2O and the combined organics were dried (Na2SO4), filtered, and concentrated to a brown foam. Trituration with hexanes/Et2O afforded the title compound (0.222 g) in good purity: MS (ES) m/z 285 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673948B2
Source datasetuspto-grants-2014_03
ORD IDord-afe8fb9ea13249d0825734ab7ac9aa2a
Source noteuspto-grants-2014_03