Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46781Generated: October 25, 2026

4-Phenoxyphenol → 2-(4-Phenoxyphenoxy)cyclopentan-1-ol

https://huagongshe.com/reaction/46781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenoxyphenolHCID 13254—
ReactantTriethylammonium iodideHCID 3014304—
SolventChloroformHCID 6212—
Product2-(4-Phenoxyphenoxy)cyclopentan-1-olHCID 22247676—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 18.6 g of 4-phenoxyphenol, 12.8 g of 1,2-carbonyldioxycyclopentane and 4.6 g of triethylammonium iodide is stirred for 7 hours at 150° C. After cooling, the reaction mixture is taken up in chloroform. The solution is washed with water and once with saturated sodium chloride solution, dried over sodium sulphate and concentrated by rotary evaporation. Fractional distillation of the residue yields (2-(4-phenoxyphenoxy)-cyclopentan-1-ol as a colourless oil with a melting point of 181°-185° C./0.001 torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04175137
Source datasetuspto-grants-1979_11
ORD IDord-548d1b3741fe4d498d99cad709f385ba
Source noteuspto-grants-1979_11