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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963748Generated: October 30, 2026

Gamma-Butyrolactone → HCID 131730505, compound

https://huagongshe.com/reaction/1963748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGamma-ButyrolactoneHCID 7302—
Reactantalpha,alpha'-Dichloro-p-xyleneHCID 12171—
Reactant9,9-Bis(4-hydroxyphenyl)fluoreneHCID 76716—
ReactantAluminum(III) ChlorideHCID 6451240—
ProductHCID 131730505HCID 131730505—

Reaction Steps

8.75 g (0.05 mol) of α,α′-dichloro-p-xylene, 26.66 g of aluminum chloride, and 200 g of γ-butyrolactone were introduced into 1 l 4-neck flask having a mechanical agitator, a condenser, 300 ml add in a dropwise funnel, and a nitrogen gas inlet and well stirred while flowing nitrogen gas in. After 10 minutes, 35.03 g (0.10 mol) of 4,4′-(9-fluorenylidene)diphenol was dissolved into 200 g of γ-butyrolactone to provide a solution. The solution was slowly dripped for 30 minutes and reacted for 12 hours. After completing the reaction, the acid was removed by using water and condensed by an evaporator. Then it was diluted by using methylamylketone (MAK) and methanol to provide a solution of MAK/methanol=4/1 (weight ratio) having a concentration of 15 wt %. The solution was introduced into 3 l separating funnel and added with n-heptane to removed a low molecular weight-containing monomer to provide a polymer (Mw=12,000, polydispersity=2.0) represented by the following Chemical Formula 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415424B2
Source datasetuspto-grants-2013_04
ORD IDord-0f145fef390347e28f30476f34175977
Source noteuspto-grants-2013_04