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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768879Generated: October 31, 2026

3,4-dihydro-2H-pyran → 2H-Pyran, tetrahydro-2-(4-iodophenoxy)-

https://huagongshe.com/reaction/1768879

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactant4-IodophenolHCID 10894—
SolventHexaneHCID 8058—
Product2H-Pyran, tetrahydro-2-(4-iodophenoxy)-HCID 291680377%

Reaction Steps

In 1 l of four-necked flask, 178 g (0.81 mol) of p-iodophenol, 81.68 g of dihydropyran and hexane were introduced and stirred for one hour. Then, 15 g of a cation exchange resin Amberlyst 15 (Rohm & Haas Co. "Amberlyst"®) was added thereto and stirred at room temperature overnight. Amberlyst 15 was removed by filtration and the filtrate was washed with an alkali and then with water. The oil layer was dried over sodium hydroxide and the solvent was distilled off to obtain 189.7 g (yield: 77%) of 4-[(tetrahydropyran-2-yl)oxy]iodobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380461
Source datasetuspto-grants-1995_01
ORD IDord-b6f90781102743f783824218a542614e
Source noteuspto-grants-1995_01