Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402428Generated: October 30, 2026

Methanol → 1-(4-Fluorophenyl)-4-methyl-1H-1,2,3-triazole

https://huagongshe.com/reaction/402428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(4-Fluorophenyl)-4-methyl-5-piperidino-4,5-dihydro-1,2,3-triazoleHCID 19914654—
SolventWaterHCID 962—
Product1-(4-Fluorophenyl)-4-methyl-1H-1,2,3-triazoleHCID 1991468878.3%

Reaction Steps

Prepared in analogy to EP 0 433 842 A2. A mixture of 1-[3-(4-fluoro-phenyl)-5-methyl-4,5-dihydro-3H-[1,2,3]triazol-4-yl]-piperidine (1.15 g, 0.004 mol) and potassium hydroxide in MeOH (2 N, 29.2 mL, 58 mmol) was heated under reflux for 6 h then cooled to room temperature. The mixture was then poured into water and extracted with diethyl ether and the combined organic extracts washed with brine, dried over sodium sulphate, filtered and evaporated to give the title product (555 mg) as a white solid. The filtrate was evaporated and purification by chromatography (silica, 10 to 60% ethyl acetate in heptane) afforded the title compound (41 mg, 79%) as an off white solid. Total yield (596 mg, 77%). MS: m/e=178.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742097B2
Source datasetuspto-grants-2014_06
ORD IDord-1f8b98b54cff4fe68c084928cab1b47b
Source noteuspto-grants-2014_06