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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107609Generated: October 31, 2026

Palmitoyl chloride → N,N'-bis(2-hydroxyethyl)-N-palmitoyl-N'-oleoyl-1,2-diaminoethane

https://huagongshe.com/reaction/1107609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPalmitoyl chlorideHCID 8206—
ReactantOleoyl chlorideHCID 5364783—
ReactantMagnesium monoxideHCID 6850729—
Reactant1,2-bis(N-(2-hydroxyethyl)-palmitoylamino)ethaneHCID 18787717—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductN,N'-bis(2-hydroxyethyl)-N-palmitoyl-N'-oleoyl-1,2-diaminoethaneHCID 86755402348.5%

Reaction Steps

Into a 500 ml rounded-flask, were introduced 4.0 g of magnesium oxide and 80 g of distilled water. The mixture was stirred. Thereto was added 7.3 g of N,N'-bis(2-hydroxyethyl)-1,2-diaminoethane prepared in Example 27, and then was added 250 ml of 1,4-dioxane. 13.4 g of palmitoyl chloride was gradually added dropwise to the resulting mixture for 1 hour under violent stirring at 10° C. After stirring for 2 hours at 10° C., 14.7 g of oleoyl chloride was gradually added dropwise thereto for 1 hour. After stirring for 2 hours, the mixture was filtered, and then the filtrate was mixed with 200 ml of chloroform, and washed twice with 200 ml of distilled water. The organic phase was cooled to produce solid material, which was recovered by filtration. The solid material was dried and recrystallized from acetone, to give 26.5 g of the title compound as white powder, which was identified by IR and NMR. The results are shown in Table 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060612
Source datasetuspto-grants-2000_05
ORD IDord-0a2da7d39cb44720a19dcb2a7f598bb2
Source noteuspto-grants-2000_05