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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530154Generated: October 26, 2026

2-Chloroethyl vinyl ether → 1-Cyclohexyl-4-[2-(ethenyloxy)ethoxy]benzene

https://huagongshe.com/reaction/1530154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl vinyl etherHCID 8074—
ReactantTriethylamineHCID 8471—
Reactant4-CyclohexylphenolHCID 14327—
ReactantSodium HydroxideHCID 14798—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product1-Cyclohexyl-4-[2-(ethenyloxy)ethoxy]benzeneHCID 22011687—

Reaction Conditions

Temperature120 °C

Reaction Steps

p-Cyclohexylphenol (83.1 g (0.5 mol)) was dissolved in 300 ml of toluene, and 150 g of 2-chloroethyl vinyl ether was added thereto. Furthermore, 25 g of sodium hydroxide, 5 g of tetrabutylammonium bromide and 60 g of triethylamine were added, and the resulting mixture was heated with stirring at 120° C. for 5 hours. The reaction solution was washed with water, and excess chloroethyl vinyl ether and toluene were removed by distillation under reduced pressure. From the obtained oil, the objective p-cyclohexylphenoxyethyl vinyl ether (X-1) was obtained by distillation under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090722B2
Source datasetuspto-grants-2015_07
ORD IDord-9a25d57c76dd446f8ce17c907f969ed5
Source noteuspto-grants-2015_07