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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451010Generated: October 29, 2026

Dimethyl Sulfoxide → 3-chloro-1-(2-methoxy-4-nitrophenyl)-1H-1,2,4-triazole

https://huagongshe.com/reaction/451010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(3-chloro-1H-1,2,4-triazol-1-yl)-5-nitrophenolHCID 58075282—
SolventWaterHCID 962—
Product3-chloro-1-(2-methoxy-4-nitrophenyl)-1H-1,2,4-triazoleHCID 5807574065.6%

Reaction Steps

Iodomethane (0.860 mL, 13.82 mmol) was added to a mixture of 2-(3-chloro-1H-1,2,4-triazol-1-yl)-5-nitrophenol (1.33 g, 5.53 mmol), potassium hydroxide (0.388 g, 6.91 mmol), and DMSO (25 mL). The mixture was left to stir at rt for 24 h. The reaction mixture was poured into water (250 mL) and extracted with EtOAc (3×100 mL). The combined extracts were washed with water, washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude residue was purified using silica gel column chromatography (0-1% MeOH/chloroform, linear gradient over 72 min, flow 25 mL/min). The pure fractions were combined and concentrated to afford 3-chloro-1-(2-methoxy-4-nitrophenyl)-1H-1,2,4-triazole (0.924 g, 3.63 mmol, 65.6% yield) as a light yellow solid. LC-MS (M+H)+=255.0. 1H NMR (500 MHz, CDCl3) δ ppm 8.35 (s, 1H) 7.36 (d, J=8.55 Hz, 1H) 6.29-6.34 (m, 2H) 3.80 (s, 3H) 2.46 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486952B2
Source datasetuspto-grants-2013_07
ORD IDord-464ff98f90a5433f9984d05e6a2ee977
Source noteuspto-grants-2013_07