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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703301Generated: October 29, 2026

Methyl iodide → HCID 14672062, compound

https://huagongshe.com/reaction/703301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-Bromo-6-(trifluoromethyl)phenolHCID 14672061—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 14672062HCID 14672062—

Reaction Conditions

Temperature-78 °C

Reaction Steps

t-Butyllithium (1.7 ml of a 1.8M solution of hexane; 3 equiv.) is added to THF (1 ml) and cooled to -78° C. under argon with stirring, and a solution of 2-bromo-6-trifluoromethylphenol in dry THF (1 ml; 1 mmol) is added dropwise via syringe. The reaction is stirred 30 minutes, and then iodomethane (340 mg; 2.4 equiv.) is added dropwise via syringe at -78° C. under argon, with stirring. The mixture is allowed to warm to 0° C. with stirring over 15 minutes, and stirring is continued for 45 minutes more. The reaction is then quenched with 1N HCl (3 ml) and extracted from 1N HCl (10 ml) with 3×10 ml portions of ether. The combined ether portions are washed with water (3×20 ml portions: pH tests neutral), and the solution is then dried (MgSO4), filtered, and concentrated in vacuo to give crude 2-methyl-6-trifluoromethylphenol, which is chromatographed on silica gel with 5% ether in petroleum ether to give pure product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04982006
Source datasetuspto-grants-1991_01
ORD IDord-0badd9f971754f38ae04a4bb0b8755fc
Source noteuspto-grants-1991_01