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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486686Generated: October 30, 2026

Methyl iodide → HCID 22414475, compound

https://huagongshe.com/reaction/486686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
Reactantn-Butyl lithiumHCID 61028—
ReactantN-(4-(trifluoromethyl)phenyl)pivalamideHCID 2774289—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
ProductHCID 22414475HCID 22414475—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a chilled (28° C.) solution of 4.91 g of 2,2-dimethyl-N-(4-trifluoromethylphenyl)propanamide and 80 ml tetrahydrofuran, was added over two mins, 18.5 ml of a 2.5M solution of N-butyllithium in hexane, with stirring. The reaction mixture was stirred for two hours at 0° C. and added, dropwise over eight minutes, to a solution of 3.19 g of iodomethane and 7 ml of hexane, keeping the temperature between -2° C.+1° C. The solution was stirred for 45 mins (internal temperature reached 18° C.). Water (20 ml) was added and the mixture was extracted with dichloromethane. The combined organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated. The mixture was separated by preparative HPLC (Waters Associates Prep LC/System 500, silica gel, sample applied in and eluted with methylenechloride, 200 ml/min flow rate). The appropriate fractions were combined, concentrated, and the residue was recrystallized from toluene to give 2.23 g of product, mp 111°-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292760
Source datasetuspto-grants-1994_03
ORD IDord-1ca7b91f0d1d48819fc8b8f8e23f19d1
Source noteuspto-grants-1994_03