HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700885Generated: November 1, 2026
2,6-Di-tert-butyl-4-methylphenol → 3-[4-[2-(N-Dodecyl-N-methylamino)ethoxy]-2-vinylphenyl]propanoic acid, methyl ester
https://huagongshe.com/reaction/1700885
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Tri(butyl)vinyltin | HCID 53438229 | — |
| Reactant | 3-[4-[2-(N-Dodecyl-N-methylamino)ethoxy]-2-[trifluoromethanesulfonyloxy]phenyl]propanoic Acid, Methyl Ester | HCID 86757119 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-[4-[2-(N-Dodecyl-N-methylamino)ethoxy]-2-vinylphenyl]propanoic acid, methyl ester | HCID 86757118 | 82% |
Reaction Steps
To a solution of 3-[4-[2-(N-dodecyl-N-methylamino)ethoxy]-2-[trifluoromethanesulfonyloxy]-phenyl]propanoic acid, methyl ester (250 mg, 0.48 mmol) in 1,4-dioxane (2.5 ml) were added tributylvinyltin (1.2 ml, 4.0 mmol), lithium chloride (123 mg, 1.44 mmol), tetrakis(triphenylphosphine)-palladium(0) (10 mg) and 2,6-di-tert-butyl-4-methylphenol (10 mg). The resulting mixture was then stirred at 100° C. for 5 h. After cooling to r.t., the mixture was diluted with diethyl ether, washed with water, brine, dried over magnesium sulfate and concentrated in vacuo. The residue was chromatographed on silica gel (diethyl ether/acetone 100:0 to 80:20) to afford the title compound (170 mg, 80%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350892B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-e64aeeae9b4c41fdb65229373f0741ce |
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| Source note | uspto-grants-2002_02 |
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