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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110222Generated: October 26, 2026

Sodium Iodide → Methyl 2-[(2-methoxy-2-oxoethyl)amino]acetate

https://huagongshe.com/reaction/1110222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
Reactant5-amino-N,N'-didecyl-1,3-benzenedicarboxamideHCID 19388948—
CatalystTetrabutylammonium BromideHCID 74236—
ProductMethyl 2-[(2-methoxy-2-oxoethyl)amino]acetateHCID 428827—

Reaction Steps

A mixture of 10.0 g (0.022 mol) of 5-amino-N,N'-didecyl-1,3-benzenedicarboxamide, 31 ml (0.33 mol) of methyl bromoacetate, 6.6 g (0.044 mol) of sodium iodide, 6.1 g (0.044 mol) of potassium carbonate and 0.32 g (0.001 mol) of tetrabutylammonium bromide in 100 ml of DMF was stirred and heated at 100° for 67 hours. The reaction mixture was concentrated on the oil pump and 100 ml of saturated NaHCO3 solution was added to the residue. The product was extracted with ethyl acetate and the extract was washed with 10% sodium bisulfite solution. The dried extract was concentrated at reduced pressure to an oil which was purified by HPLC using 35% ethyl acetate-toluene. The combined pure fractions were crystallized from methanol-water to give 8.2 g (63% yield, mp 71°-75°) of N-[3,5-bis[decylamino)carbonyl]phenyl]-N-(2-methoxy-2-oxoethyl)glycine methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324747
Source datasetuspto-grants-1994_06
ORD IDord-9cdd9106293840598f5b4602ae9edcd7
Source noteuspto-grants-1994_06