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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340870Generated: October 25, 2026

Potassium Iodide → 2,5-Dimethylhexane-2,5-diyl bis(2-hydroxyacetate) isophthaloyl chloride

https://huagongshe.com/reaction/340870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantIsophthaloyl chlorideHCID 7451—
ReactantDabcoHCID 9237—
ReactantButanediolHCID 165788—
Reactant2,5-Dimethylhexane-2,5-diyl bis(2-hydroxyacetate)HCID 58282118—
SolventPyridineHCID 1049—
Product2,5-Dimethylhexane-2,5-diyl bis(2-hydroxyacetate) isophthaloyl chlorideHCID 86654795—

Reaction Steps

A solution of 2,5-dimethylhexane-2,5-diyl bis(2-hydroxyacetate) (69) (0.997 g, 3.8 mmol), isophthaloyl chloride (115) (0.812 g, 4.0 mmol), a catalytic amount of 1,4-diazabicyclo[2.2.2]octane, and a catalytic amount of potassium iodide in 20 mL of pyridine was brought to 50° C. while stirring under nitrogen. After 24 hours, butanediol (0.072 g, 0.8 mmol) diluted in 10 mL of pyridine was added to the reaction mixture using a syringe pump over 8 hours. The solution was then quenched in 200 mL of cold 1N hydrochloric acid. The polymer precipitate is collected by filtration, redissolved in tetrahydrofuran, and precipitated in 100 mL of cold 1N hydrochloric acid. The polymer is then collected by filtration and dried under high vacuum. The polymer was found to have a molecular weight of ˜14,000 g/mol by GPC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895691B2
Source datasetuspto-grants-2014_11
ORD IDord-f295ad751c774e79b7051715696ade2c
Source noteuspto-grants-2014_11