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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757804Generated: October 26, 2026

Sodium Iodide → N-(2-methoxy-2-oxoethyl)-N-[3-[(Z)-(9-octadecenyl)oxy]phenyl]glycine methyl ester

https://huagongshe.com/reaction/1757804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant9-Octadecene, 1-bromo-, (9Z)-HCID 5840383—
Reactant3-hydroxyphenyl-N-(2-methoxy-2-oxoethyl)glycine methyl esterHCID 19389047—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
ProductN-(2-methoxy-2-oxoethyl)-N-[3-[(Z)-(9-octadecenyl)oxy]phenyl]glycine methyl esterHCID 6778812252.2%

Reaction Steps

A mixture of 0.24 g (0.95 mmol) of N-(3-hydroxyphenyl)-N-(2-methoxy-2-oxoethyl)glycine methyl ester, 0.33 g (1 mmol) of oleyl bromide, 0.15 g (1 mmol) of sodium iodide and 0.41 g (3 mmol) of potassium carbonate in 10 ml of acetone was stirred at reflux under argon for 18 hours. DMF (5 ml) was added and reflux was continued for 3 days. The solvents were removed at reduced pressure and the residue was dissolved in ethyl acetate. The extract was dried and concentrated at reduced pressure to an oil which was purified by chromatography on 230-400mesh silica gel using 25% ethyl acetate-hexane to give 0.25 g (50% yield, mp 36°-37°) of N-(2-methoxy- 2-oxoethyl)-N-[3-[(Z)-(9-octadecenyl)oxy]phenyl]glycine methyl ester. The nmr and mass spectra were consistent with the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446189
Source datasetuspto-grants-1995_08
ORD IDord-41c745b7deb4422e9cd3acb473d80a11
Source noteuspto-grants-1995_08