Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295530Generated: October 30, 2026

Sulfuric Acid → HCID 86586297, compound

https://huagongshe.com/reaction/1295530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantButylamineHCID 8007—
ReactantOctanoyl chlorideHCID 8124—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18601051HCID 18601051—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 86586297HCID 86586297—

Reaction Conditions

Temperature90 °C

Reaction Steps

110 g of sodium glutamate monohydrate was dissolved in 140 g of water and 78 g of 27% aqueous sodium hydroxide and cooled to 10° C. The solution was added with 110 g of acetone and added dropwise with 87 g of octanoyl chloride and 90 g of 27% aqueous sodium hydroxide. The reaction mixture for the acylation was diluted with 100 g of water and neutralized with 64 g of 95% sulfuric acid to separate an oil. The aqueous layer was removed, and the oil layer was concentrated under reduced pressure to obtain an oily substance. The resulting oily substance was dissolved in 742 g of methanol, and the solution was added with 6.2 g of 95% sulfuric acid and refluxed for 9 hours. The reaction mixture was left stand for cooling to 35° C. and neutralized with 10.5 g of n-butylamine, and then the methanol was evaporated to obtain an oily substance. The resulting oily substance was added with 630 g of toluene and 191 g of n-butylamine and the mixture was stirred with heating at 90° C. for 10 hours. The reaction mixture was added with 500 g of warm water and 178 g of 95% sulfuric acid to separate an oil, and the aqueous layer was removed. The oil layer was added with 645 g of warm water, and the solvent was removed under ordinary pressure to obtain slurry of white solid. The resulting solid was collected by filtration and dried in vacuo at 50° C. to obtain octanoylglutamic acid dibutylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244419B2
Source datasetuspto-grants-2007_07
ORD IDord-6da8acb67a684f109e9590f74fc1dcb6
Source noteuspto-grants-2007_07