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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457574Generated: October 30, 2026

Triethylamine → {2-[3-(1,1-Dimethylundecyl)ureido]-4-methoxy-6-tert-butylphenoxy}methoxymethane

https://huagongshe.com/reaction/1457574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2,2-Dimethyldodecanoic acidHCID 4265726—
Reactant(2-Amino-4-methoxy-6-tert-butylphenoxy)methoxymethaneHCID 18765846—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product{2-[3-(1,1-Dimethylundecyl)ureido]-4-methoxy-6-tert-butylphenoxy}methoxymethaneHCID 22099452—

Reaction Steps

A mixture of 5 g of 2,2-dimethyllauric acid, 4.72 ml of diphenylphosphorylazide (DPPA), 3.36 ml of triethylamine and 80 ml of benzene was refluxed for one hour. After cooling, a mixed solution of 5.763 g of (2-amino-4-methoxy-6-tert-butylphenoxy)methoxymethane and 20 ml of benzene was added dropwise to the above mixture. The resulting mixture was stirred at room temperature for one hour and then under reflux for 10 hours. Water was added to the reaction mixture, and the reaction mixture was extracted with ethyl acetate. The extract was washed and dried, and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (solvent; hexane:ethyl acetate=4:1) and the product was recrystallized from hexane to give 2.89 g of {2-[3-(1,1-dimethylundecyl)ureido]-4-methoxy-6-tert-butylphenoxy}methoxymethane (melting point: 83°-85° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849732
Source datasetuspto-grants-1998_12
ORD IDord-18e8b5c3d7bc4257a1aa16d682bbc4bf
Source noteuspto-grants-1998_12