Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459147Generated: October 31, 2026

Acetone → HCID 22940783, compound

https://huagongshe.com/reaction/1459147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
ReactantDodecanoyl chlorideHCID 8166—
Reactant3929-61-1HCID 439500—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 22940783HCID 2294078392.2%

Reaction Conditions

Temperature10 °C

Reaction Steps

A suspension of 20 g (0.0724 mols) of α-glutamylglutamic acid in 70 ml of water was dissolved in a 27-% sodium hydroxide aqueous solution until the pH reached 11, and 35 ml of acetone were added thereto. To the solution were added dropwise 15.8 g (0.0724 mols) of lauroyl chloride over a period of 1 hour. When adding lauroyl chloride, the temperature was maintained at 10° C., and 27-% sodium hydroxide was added dropwise simultaneously to keep the pH constant. After the addition of lauroyl chloride, the reaction solution was warmed at 30° C., and allowed to stand for 30 minutes. Subsequently, the pH was adjusted to 1 with the addition of conc. hydrochloric acid. The solid precipitate was separated by filtration, and dried to obtain 30.6 g of N-(N'-lauroyl-α-glutamyl)glutamic acid in a yield of 92%. This solid was analyzed by infrared spectrophotometry. A peak diagnostic of an amide group was observed at 1,650 cm-1 and a peak diagnostic of a carboxyl group was observed at 1,730 cm-1, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854199
Source datasetuspto-grants-1998_12
ORD IDord-e98289a636204636ace0d187bb8c5477
Source noteuspto-grants-1998_12