Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784325Generated: October 30, 2026

p-(1-Ethoxyethoxy)styrene → HCID 69084924, compound

https://huagongshe.com/reaction/1784325

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(1-Ethoxyethoxy)styreneHCID 9855712—
ReactantHCID 23084984HCID 23084984—
CatalystButyllithiumHCID 178418339—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69084924HCID 69084924148%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a reaction vessel, 111.2 g (0.5 mol) of 3-methoxy-4-(1-ethoxyethoxy)styrene purified by distillation and 96.1 g (0.5 mol) of 4-(1-ethoxyethoxy)styrene (produced by Tosoh Corp.) were dissolved in 500 ml of dehydrated tetrahydrofuran. While stirring the resulting solution, a nitrogen gas was passed into the system and after cooling the system to −78° C., 0.02 mol of n-butyl lithium was added thereto and the polymerization was initiated. The polymerization degree was confirmed by sampling a part of the reaction solution every 30 minutes. When a desired polymerization degree was achieved, the polymerization was stopped by adding methanol to the reaction solution. After waiting until the reaction solution was cooled to room temperature, the reaction solution was added dropwise in 5 L of methanol to precipitate a polymer. The solid obtained by filtration was dissolved in 300 ml of acetone and again added dropwise in 5 L of methanol and after filtration, the solid obtained was dried under reduced pressure to obtain 153.4 g of a [3-methoxy-4-(1-ethoxyethoxy)styrene]-[4-(1-ethoxyethoxy)styrene] copolymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504193B2
Source datasetuspto-grants-2009_03
ORD IDord-2978a0369c104991a56a0422e78377f2
Source noteuspto-grants-2009_03