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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485986Generated: October 29, 2026

Hydrochloric Acid → p-(1-Trifluoromethylheptyloxy)iodobenzene

https://huagongshe.com/reaction/485986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
Reactantp-(1-Trifluoromethylheptyloxy)-anilineHCID 15123948—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Productp-(1-Trifluoromethylheptyloxy)iodobenzeneHCID 15123949—

Reaction Steps

To 200 ml of water containing 25 g of 36% hydrochloric acid, were added 6.7 g of oa p-(1-trifluoromethyl-heptyloxy)-aniline, and cooled to a temperature below 5° C., followed by adding thereto dropwise 1.7 g of sodium nitrite dissolved in 10 ml of water. After the addition was over, stirring was continued for an hour, and then 20 g of potassium iodide dissolved in 20 ml of water were added thereto, followed by putting back the temperature gradually to room temperature and stirring was continued until no evolution of nitrogen was observed. After completion of the reaction, the product was extracted with hexane. The hexane phase was washed subsequently with water, an aqueous solution of sodium hydrogen sulfite and then water, followed by distilling off the hexane to obtain 77 g of oily oa p-(1-trifluoromethylheptyloxy)iodobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290478
Source datasetuspto-grants-1994_03
ORD IDord-be1fa85db660458dbe5a141cf136221e
Source noteuspto-grants-1994_03