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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258875Generated: November 1, 2026

Methyl iodide → 4-(4-Fluoro-phenyl)-1-methyl-1H-[1,2,3]triazole

https://huagongshe.com/reaction/1258875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium AzideHCID 33557—
Reactant1-Ethynyl-4-fluorobenzeneHCID 522627—
Reactantsodium L-ascorbic acidHCID 66586226—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-(4-Fluoro-phenyl)-1-methyl-1H-[1,2,3]triazoleHCID 67495571286.4%

Reaction Conditions

Temperature75 °C

Reaction Steps

The reaction mixture was splitted in 24 tubes of 1.00 g (8.32 mmol) each. A mixture of 1-ethynyl-4-fluorobenzene (24.0 g, 200 mmol), sodium azide (14.41 g, 222 mmol), iodomethane (14.93 mL, 240 mmol), copper(I) iodide (8.03 g, 42 mmol) and L-(+)-ascorbic acid sodium salt (7.84 g, 40 mmol) in water (240 mL) was heated at 75° C. for 10 h. The mixture was then diluted with dichloromethane (25 mL) and filtered off. The aqueous layer of the filtrate was extracted with dichloromethane and the combined organic extracts washed with brine, dried over sodium sulphate, filtered and evaporated. Purification by chromatography (silica, 0 to 5% methanol in dichloromethane) afforded the title compound (20.3 g, 57%) as a white solid after recrystallisation from ethyl acetate-heptane. MS: m/e=178.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466181B2
Source datasetuspto-grants-2013_06
ORD IDord-1d974565c289454c935064bc6155bee9
Source noteuspto-grants-2013_06