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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2,2-Dimethyldodecanoic acid | HCID 4265726 | — |
| Reactant | (2-Amino-4-methoxy-6-tert-butylphenoxy)methoxymethane | HCID 18765846 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | {2-[3-(1,1-Dimethylundecyl)ureido]-4-methoxy-6-tert-butylphenoxy}methoxymethane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849732 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-18e8b5c3d7bc4257a1aa16d682bbc4bf |
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| Source note | uspto-grants-1998_12 |
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