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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269200Generated: October 31, 2026

Methyl iodide → 3-Bromo-2,6-difluorotoluene

https://huagongshe.com/reaction/2269200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
Reactant1-Bromo-2,4-difluorobenzeneHCID 67674—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-2,6-difluorotolueneHCID 11287226—

Reaction Steps

Diisopropylamine (11.9 ml, 85 mmol) is dissolved in 50 ml of anhydrous THF and cooled in a dry ice/acetone bath. n-Butyllithium (34 ml of a 2.5 M solution in hexanes, 85 mmol) is added dropwise. After 15 minutes, a solution of 1-bromo-2,4-difluorobenzene (16 g, 83 mmol) in 8 ml of THF is added at a rate to keep the temperature below −65° C. The reaction is stirred for 2.5 hours then a solution of iodomethane (10.3 ml, 166 mmol) in 8 ml of THF is added to the reaction. The ice bath is removed and the reaction is allowed to warm to room temperature. After 2 hours the reaction is quenched with water and 1N HCl. The aqueous layer is extracted twice with ether. The combined organics are washed with brine and dried over Na2SO4. Removal of the solvent affords the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329391B1
Source datasetuspto-grants-2001_12
ORD IDord-7f713a8c26de4622b439878e1b43ad99
Source noteuspto-grants-2001_12