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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262341Generated: November 1, 2026

Sulfuric Acid → N~2~-Dodecanoyl-L-glutamine

https://huagongshe.com/reaction/2262341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantL-GlutamineHCID 5961—
ReactantDodecanoyl chlorideHCID 8166—
ReactantSodium HydroxideHCID 14798—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductN~2~-Dodecanoyl-L-glutamineHCID 16213882—

Reaction Steps

108 g of L-glutamine was dissolved in 343 g of water and 102 g of aqueous 27% sodium hydroxide solution, and cooled to 10° C. 138 g of acetone was added, and 152 g of lauroyl chloride and 108 g of aqueous 27% sodium hydroxide solution were dropwise added. 300 g of the acylation liquid was diluted with water, neutralized with 35 g of 75% sulfuric acid, and filtered to obtain a white powder substance, N-lauroyl-L-glutamine. 367 g of isopropyl alcohol and 30 g of 95% sulfuric acid were added to 101.7 g of the product, and refluxed for 3.5 hours. After solvent removal, 350 g of isopropyl alcohol was added to it, and refluxed for 3 hours. After further solvent removal, 350 g of isopropyl alcohol was added and refluxed for 4 hours. The reaction liquid was left cooled to 35° C., and a white solid was collected by filtration, and dried in vacuum at 50° C. to obtain 73.14 g of a crude crystal of N-lauroyl-L-glutamine isopropyl ester (N-lauroyl-L-glutamine isopropyl ester/2-(lauroylamino)glutarimide/isopropyl N-lauroyl-2-pyrrolidone-5-carboxylate/diisopropyl N-lauryl-L-glutamate (ratio by weight)=100/16/9/16). Further, this was recrystallized from acetone to obtain 30.00 g of a pure crystal of N-lauroyl-L-glutamine isopropyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07850955B2
Source datasetuspto-grants-2010_12
ORD IDord-0137aaee08de4011b422ebb14216f0ad
Source noteuspto-grants-2010_12