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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855322Generated: October 31, 2026

Potassium Hydroxide → 1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazole

https://huagongshe.com/reaction/1855322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-Chloro-5-nitroanisoleHCID 70519—
ReactantHCID 178418800HCID 178418800—
SolventDimethyl SulfoxideHCID 679—
Product1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazoleHCID 4548018045.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 2-chloro-5-nitroanisole (187 mg, 1 mmol), of 4-methyl-1H-imidazole (335 mg, 4 mmol) and of potassium hydroxide (99 mg, 1.5 mmol) in DMSO (0.86 mL) was stirred for 5 h at 80° C. under an atmosphere of nitrogen. After cooling to 20° C. the reaction was poured onto ice-water. A precipitation was formed and the suspension was stirred for 15 min. The solid was filtered off, washed with water, dissolved in dichloromethane, dried over sodium sulfate, filtered and the solvent was evaporated under reduced pressure to yield a yellow solid. The crude product was purified on silica gel using dichloromethane/methanol (19:1 v/v) as eluent to yield the title compound (106 mg, 45%) as a pale-yellow solid. Alternatively the product can be also crystallized from the crude material from diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-76dec119d4124e7781fe6e3cd4f8326c
Source noteuspto-grants-2015_02