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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290016Generated: November 2, 2026

Ethylene Glycol → Bis(2-hydroxyethyl) terephthalate

https://huagongshe.com/reaction/1290016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantTerephthalic AcidHCID 7489—
Reactant1,4-CyclohexanedimethanolHCID 7735—
ProductBis(2-hydroxyethyl) terephthalateHCID 13739—

Reaction Steps

The poly(ethylene terephthalate) and poly(ethylene terephthalate-co-1,4-cyclohexanedimethylene terephthalate) polyesters described in Tables 1 and 2 were prepared by standard melt polymerization techniques known to the art. Terephthalic acid, ethylene glycol and 1,4-cyclohexanedimethanol (CHDM) were first pre-esterified to form the bis(2-hydroxyethyl)terephthalate or the equivalent CHDM co-terephthalate monomers in a pressurized vessel. This was required due to the high temperature necessary to dissolve terephthalic acid in the polyhydric alcohols. However, this should not be limited to such a procedure, as a continuous process, or any other polyester synthesis based on TPA (terephthalic acid) known the art, could also be used. Once formed, the monomers were added to a 4-necked 500 mL round bottom glass flask which was equipped with a nitrogen inlet, an additive inlet, a condensate outlet and a stirrer. Catalysts, stabilizers and toner dyes, as indicated in Table 1, were also added to this same reaction vessel. The reaction flask was then purged with nitrogen and then immersed in a metal bath which was preheated to 225° C. The mixture was stirred and held at this temperature for 15 minutes to form a homogeneous melt. The temperature was then raised to 280° C. and vacuum was applied incrementally until a vacuum of <1 mm Hg was obtained. The reaction mixture was stirred and maintained under these conditions for 45 minutes. The formed polyester was then isolated, and analyzed for color, molecular weight, and thermal stability.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750635
Source datasetuspto-grants-1998_05
ORD IDord-13ef944d5cbd410a9c3391f486ece1d9
Source noteuspto-grants-1998_05