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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383942Generated: November 2, 2026

Methyl iodide → 3-Bromo-4-methyl-5-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/2383942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
Reactant3-Bromo-5-(trifluoromethyl)pyridineHCID 11127991—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-Bromo-4-methyl-5-(trifluoromethyl)pyridineHCID 5963617517.92%

Reaction Conditions

Temperature-10 °C

Reaction Steps

n-Butyl Lithium (1.9 mL, 3.044 mmol) was added to a solution of DIPA (335.7 mg, 3.318 mmol) in THF (6 mL) at -78° C. The reaction mixture was stirred at -10° C. for 10 minutes. This was followed by the addition of 3-bromo-5-trifluoromethyl-pyridine (500 mg, 2.212 mmol) in THF (3 mL) at -100° C. The reaction mixture was stirred for a further 15 minutes at -90° C. and was followed by the addition of methyl iodide (557.0 mg, 3.924 mmol) in THF (2 mL) at -78° C. with stirring over a period of 30 minutes. The reaction was monitored by TLC (5% ethyl acetate in hexane). The reaction mixture was quenched with aqueous NaHCO3 solution and extracted with ethyl acetate (100 mL). The organic layer was dried over Na2SO4 and concentrated. Purification by column chromatography on silica gel (2% ethylacetate in hexane) afforded 95 mg of the product (17.92% yield). LCMS: m/z=239.8 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263635B2
Source datasetuspto-grants-2012_09
ORD IDord-2daa4fea9e3f48028177dd6fe2def8e0
Source noteuspto-grants-2012_09