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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540987Generated: October 30, 2026

Hexanoic Acid → HCID 131731981, compound

https://huagongshe.com/reaction/540987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexanoic AcidHCID 8892—
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant56491-53-3HCID 19708237—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131731981HCID 131731981—

Reaction Steps

Into a 250 mL vessel, tetraglycerol (5.0 g, 15.91 mmol) was added and dissolved into anhydrous THF (50 mL). Hexanoic acid (11.96 mL, 95.44 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 (0.194 g, 1.59 mmol) and N-hydroxysuccinimide (0.183 g, 1.59 mmol) were both dissolved in the solution. When the catalysts were fully dissolved, N,N-diisopropylcarbodiimide (15.0 mL, 97.03 mmol) was pipetted into the vessel and was sealed to keep the reaction dry. The reaction proceeded overnight at 55° C. The solution was stripped of THF via rotoevaporation and redissolved into chloroform. The organic layer was washed 2× with sodium bicarbonate buffer and 2× with deionized water to remove unreacted starting materials. The chloroform was removed to yield a clear viscous liquid. 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-c42cb1a625c44d008051ce0d4765aa41
Source noteuspto-grants-2014_10