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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459149Generated: November 1, 2026

Acetone → HCID 22940784, compound

https://huagongshe.com/reaction/1459149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
ReactantDodecanoyl chlorideHCID 8166—
ReactantL-gamma-glutamyl-L-glutamic acidHCID 92865—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 22940784HCID 2294078489%

Reaction Conditions

Temperature10 °C

Reaction Steps

A suspension of 16 g (0.058 mols) of γ-glutamylglutamic acid in 55 ml of water was dissolved in a 27-% sodium hydroxide aqueous solution until the pH reached 11, and 27 ml of acetone were added thereto. To the solution were added dropwise 12.6 g (0.058 mole) 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 at 11. After the completion of 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 23.6 g of N-(N'-lauroyl-γ-glutamyl)glutamic acid in a yield of 89%. This solid was analyzed by infrared spectrophotometry. A peak diagnostic of an amide group was observed at 1,640 cm-1 and a peak diagnostic of a carboxyl group was observed at 1,730 cm-1, respectively. FAB mass spectrum: 459 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854199
Source datasetuspto-grants-1998_12
ORD IDord-287a3bfe757b47a6a7b81b65e16c067c
Source noteuspto-grants-1998_12