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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402364Generated: October 30, 2026

Dimethylformamide → 4-(2-Fluorophenyl)-1-methyl-1H-1,2,3-triazole-5-carbaldehyde

https://huagongshe.com/reaction/402364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(2-fluorophenyl)-1-methyl-1H-1,2,3-triazoleHCID 67498553—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Fluorophenyl)-1-methyl-1H-1,2,3-triazole-5-carbaldehydeHCID 8666476287.2%

Reaction Conditions

Temperature-75 °C

Reaction Steps

To a solution of 4-(2-fluorophenyl)-1-methyl-1H-1,2,3-triazole (1.44 g, 8.1 mmol) in THF (41 mL) was added n-BuLi (1.6 M in hexane, 6.10 mL, 9.8 mmol) dropwise at −75° C. under Argon. The resulted orange solution was stirred at −75° C. for 1 h, then DMF (0.82 mL, 10.6 mmol) was added dropwise at −75° C. and the reaction mixture was allowed to warm up to room temperature over 1 h. The mixture was then poured into saturated ammonium chloride solution and extracted with ethyl acetate and the combined organic extracts washed with brine, dried over sodium sulphate, filtered and evaporated. Purification by chromatography (silica, 0 to 50% ethyl acetate in heptane) afforded the title compound (1.45 g, 87%) as an off white solid. MS: m/e=206.0 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742097B2
Source datasetuspto-grants-2014_06
ORD IDord-3755f18473d943d6acb6c400b490b90d
Source noteuspto-grants-2014_06