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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856597Generated: October 29, 2026

Iodine → 1-Cyano-4-[[(3-iodo-2-propynyl)oxy]methoxy]benzene

https://huagongshe.com/reaction/1856597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22131913HCID 22131913—
SolventMethanolHCID 887—
Product1-Cyano-4-[[(3-iodo-2-propynyl)oxy]methoxy]benzeneHCID 2213190794%

Reaction Steps

1 -Cyano-4-[(2-propynyloxy)methoxy]benzene (Intermediate II-i) (9.4 g, 0.05 mol) prepared in the above example 4 and 48% w/v aqueous sodium hydroxide solution (11.3 g) were added to methanol (75 g). Iodine (14.0 g, 0.055 mol) was then added to the solution in several portions while maintaining the inner temperature below 10° C. The reaction mixture was stirred for further 3 hours and the solvent was then evaporated off. The residue was extracted with toluene (10 ml) and the toluene layer was washed with distilled water. Toluene was then evaporated off to obtain a crude reaction product (15.3 g). The crude reaction product (15.3 g) was recrystallized from hexane (50 ml) to obtain the desired 1-cyano-4-[[(3-iodo-2-propynyl)oxy]methoxy]benzene (Derivative III-i)(12.6 g, 94% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143311
Source datasetuspto-grants-2000_11
ORD IDord-0a3ddb90068d4a629a308a3bd19daf5e
Source noteuspto-grants-2000_11