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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378450Generated: November 2, 2026

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

https://huagongshe.com/reaction/2378450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN-[4-chloro-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamideHCID 715673—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-chloro-2-methyl-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamideHCID 2187484867%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of N-(4-chloro-3-trifluoromethylphenyl)-2,2-dimethylpropionamide (2.29 g, 8.19 mmol) in anhydrous THF (25 mL) cooled to 0-5° C. was added a solution of 1.6M n-butyllithium in hexanes (12.3 mL, 19.7 mmol) slowly so that the reaction temperature was maintained below 5° C. The solution was stirred at 0-5° C. for 1.5 h. A solution of iodomethane (0.56 mL, 9.01 mmol) in petroleum ether (2 mL) was added over 20 min while maintaining the temperature below 5° C. The suspension was stirred at 0-5° C. for 1 h and diluted with water and ether. The aqueous layer was extracted with ether and the combined organic layers washed with brine, dried over MgSO4, filtered and concentrated. The residue was chromatographed (silica gel) eluting with CH2Cl2 to afford compound 760B (1.60 g, 67%). MS (ES): m/z=294 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470797B2
Source datasetuspto-grants-2008_12
ORD IDord-6bae154781d7462c87997b13295fb138
Source noteuspto-grants-2008_12