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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376811Generated: October 25, 2026

Trimethylolpropane → Cyclohexane tertiary butyl isophthalate

https://huagongshe.com/reaction/2376811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylolpropaneHCID 6510—
Reactant1,4-CyclohexanedimethanolHCID 7735—
Reactant1,4-Cyclohexanedicarboxylic acidHCID 14106—
ReactantAntimony triacetateHCID 23354—
ReactantNeopentyl glycolHCID 31344—
Reactantt-Butyl isophthalic acidHCID 19762767—
SolventEthylene GlycolHCID 174—
ProductCyclohexane tertiary butyl isophthalateHCID 86604590—

Reaction Conditions

Temperature254 °C

Reaction Steps

Synthesis of the co-cyclohexane-tbia was carried out in a batch reactor which was charged with the following raw materials: 1,4 cyclohexane dicarboxylic acid (37 kg), tertiary butyl isophthalic acid (59.9 kg), 1,4 cyclohexane dimethanol (37.8 kg), neopentyl glycol (11.2 kg), ethylene glycol (60.3 kg), trimethylol propane (0.5 kg), and antimony (III) acetate (90 g). Under a pressure of 2 atmospheres (2×105 N/m2), this mixture was heated to 254 degrees C. while removing the reaction by-product, water. After completing this reaction and removing the water, the pressure was gradually reduced to 1 torr (263 N/m2) while heating to 290° C. The condensation by-product, ethylene glycol, was continuously removed until a polymer with intrinsic viscosity of 0.72 dl/g, as measured in 60/40 wt % phenol/o-dichlorobenzene, was produced. The polymer had a glass transition temperature of about 67° C. as measured by DSC with a temperature ramp of 20° C./min. This CCH-tbia had a refractive index of 1.519 as measured with a Metricon refractometer at 632 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468204B2
Source datasetuspto-grants-2008_12
ORD IDord-9c5fc90ff6974e1790d86d72c47aef93
Source noteuspto-grants-2008_12