Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051286Generated: November 3, 2026

Imidazole → HCID 118555065, compound

https://huagongshe.com/reaction/1051286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantHCID 43657400HCID 43657400—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 118555065HCID 118555065—

Reaction Conditions

Temperature110 °C

Reaction Steps

A reaction mixture solution prepared by suspending 41.1 mg of 3-fluoro-4-hydroxybenzonitrile, 33.4 mg of isobutyl bromide and 62.2 mg of potassium carbonate in 1 mL of dimethylformamide was heated at 110° C. for 5 hours under a nitrogen atmosphere. After the addition of water to the reaction mixture solution, extraction was performed using ethyl acetate. The organic layer was washed with saline, followed by drying and concentrating under reduced pressure to obtain a crude product of 3-fluoro-4-(2-methylpropoxy)benzonitrile. (2) A reaction mixture prepared by adding 15.7 mg of sodium hydride and 24.5 mg of imidazole to the crude product of 3-fluoro-4-(2-methylpropoxy)benzonitrile obtained above and suspending the above in 1 mL of dimethylsulfoxide was heated at 110° C. for 5 hours under a nitrogen atmosphere. After the addition of water to the reaction mixture solution, extraction was performed using ethyl acetate. The organic layer was washed with saline, followed by drying and concentrating under reduced pressure to obtain a crude product of 3-(1H-imidazol-1-yl)-4-(2-methylpropoxy)benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388174B2
Source datasetuspto-grants-2016_07
ORD IDord-3c5a2c9283f44cb196ee248c27918d77
Source noteuspto-grants-2016_07