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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N-[4-chloro-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamide | HCID 715673 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[4-chloro-2-methyl-3-(trifluoromethyl)phenyl]-2,2-dimethylpropanamide | HCID 21874848 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07470797B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-6bae154781d7462c87997b13295fb138 |
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| Source note | uspto-grants-2008_12 |
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