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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404559Generated: October 31, 2026

Methyl iodide → 5-(2-bromo-4-chloro-6-fluoro-phenyl)-1-methyl-1H-tetrazole

https://huagongshe.com/reaction/1404559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(2-Bromo-4-chloro-6-fluoro-phenyl)-2H-tetrazoleHCID 67979289—
SolventDimethylformamideHCID 6228—
Product5-(2-bromo-4-chloro-6-fluoro-phenyl)-1-methyl-1H-tetrazoleHCID 6797933335%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 5-(2-bromo-4-chloro-6-fluoro-phenyl)-2H-tetrazole (4.15 g, 14.95 mmol), K2CO3 (3.1 g, 22.43 mmol) and iodomethane (1.3 ml, 20.94 mmol) in DMF (30 ml) was stirred at 25° C. for 3 h. The mixture was partitioned between EtOAc (80 ml) and water (60 ml), the organic layer was separated, washed with water and brine, dried with Na2SO4 and concentrated. The remaining residue was purified by chromatography (silica gel; hexane/EtOAc 100:0-90:10) to obtain 5-(2-bromo-4-chloro-6-fluoro-phenyl)-1-methyl-1H-tetrazole as pale yellow solid (1.5 g, 35%) and the title compound as reddish liquid (1.7 g, 39%). MS: 291.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912221B2
Source datasetuspto-grants-2014_12
ORD IDord-7d3678795d8c4617949b03ee63bb20e7
Source noteuspto-grants-2014_12