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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540985Generated: October 28, 2026

Trimethylolpropane → HCID 131731982, compound

https://huagongshe.com/reaction/540985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylolpropaneHCID 6510—
ReactantHexanoic AcidHCID 8892—
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantN-HydroxysuccinimideHCID 80170—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 131731982HCID 131731982—

Reaction Steps

Into a 250 mL vessel, hexaglycerol (5.0 g, 10.81 mmol) was added and dissolved into anhydrous DMSO (50 mL). Hexanoic acid (10.84 mL, 86.49 mmol) was also dissolved into the reaction mixture which was stirred magnetically at room temperature for one hour to fully dissolve the reagents. N,N-dimethylaminopyridine (0.132 g, 1.08 mmol) and N-hydroxysuccinimide (0.124 g, 1.08 mmol) were both dissolved in the solution. When the catalysts were fully dissolved, N,N-diisopropylcarbodiimide (13.54 mL, 87.57 mmol) was pipetted into the vessel and was sealed to keep the reaction dry. The reaction proceeded overnight at 55° C. The solution was dialyzed in SpectraPor7 MWCO 1000 dialysis tubing to remove the DMSO and unreacted monomer. The polymer crashed out in water into a thick white liquid. After 3 days of dialysis, the solution was placed into a separatory funnel and the organic portion was dissolved into chloroform. The water layer was removed and the organic layer was dried with sodium sulfate. The solvent was stripped via rotoevaporation to leave a clear thick liquid product. NMR analysis supported full conversion of hydroxyl groups to the hexanoic esters.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871819B2
Source datasetuspto-grants-2014_10
ORD IDord-e5073c3d71794580a4872c8c30b97b46
Source noteuspto-grants-2014_10